http://identifiers.org/exac.variant/19-55446027-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55446027
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55446027
    reference: chr 19
allele count: 6
allele frequency: 5.542929992794191e-5
allele num: 108246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2301G>T
  hgvsp: ENSP00000339491.2:p.Arg767Ser
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2301G>T
  hgvsp: ENSP00000468243.1:p.Arg767Ser
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2385G>T
  hgvsp: ENSP00000414273.1:p.Arg795Ser
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2217G>T
  hgvsp: ENSP00000409137.2:p.Arg739Ser
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2301G>T
  hgvsp: ENSP00000467123.1:p.Arg767Ser
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2301G>T
  hgvsp: ENSP00000465520.1:p.Arg767Ser
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2217G>T
  hgvsp: ENSP00000329568.5:p.Arg739Ser
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2301G>T
  hgvsp: ENSP00000468706.1:p.Arg767Ser
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6209
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 578
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21892
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10737
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11068
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 839
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg767Ser
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-55446028-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55446028
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55446028
    reference: chr 19
allele count: 1
allele frequency: 9.297136481963556e-6
allele num: 107560
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2301-1G>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2217-1G>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2301-1G>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2385-1G>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2301-1G>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2301-1G>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2301-1G>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2217-1G>C
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1766
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21129
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6628
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11925
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32008
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17131
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1200
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
hgvs: c.2301-1G>C
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

19-55446031-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55446031
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55446031
    reference: chr 19
allele count: 1
allele frequency: 9.488206159743439e-6
allele num: 105394
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2301-4A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2217-4A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2385-4A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2301-4A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2301-4A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2301-4A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2301-4A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2217-4A>G
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14983
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18382
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9775
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5072
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 487
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 701
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1508
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3886
  bin: 6.75e1
  variant carriers: 0
hgvs: c.2301-4A>G
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP

19-55446032-G-GA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55446032
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55446033
    reference: chr 19
allele count: 2
allele frequency: 1.90836052747085e-5
allele num: 104802
alternate allele: GA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2217-6dupT
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2301-6dupT
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2301-6dupT
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2385-6dupT
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2301-6dupT
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2217-6dupT
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2301-6dupT
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2301-6dupT
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15732
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9609
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4856
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17717
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7809
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27374
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
hgvs: c.2301-6dupT
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

19-55446033-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55446033
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55446033
    reference: chr 19
allele count: 1
allele frequency: 9.541984732824428e-6
allele num: 104800
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2385-6T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2301-6T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2217-6T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2301-6T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2301-6T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2301-6T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2301-6T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2217-6T>C
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17693
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15775
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2114
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7861
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 559
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21835
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1226
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3789
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 4.25e1
  variant carriers: 0
hgvs: c.2301-6T>C
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

19-55446034-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55446034
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55446034
    reference: chr 19
allele count: 2
allele frequency: 1.938660773137916e-5
allele num: 103164
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2301-7T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2301-7T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2217-7T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2301-7T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2301-7T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2217-7T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2385-7T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2301-7T>C
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8510
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15215
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18531
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1856
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 210
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2980
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24072
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 8.75e1
  variant carriers: 0
hgvs: c.2301-7T>C
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-55446037-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55446037
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55446037
    reference: chr 19
allele count: 1
allele frequency: 9.71722864639005e-6
allele num: 102910
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2301-10C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2301-10C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2217-10C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2301-10C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2217-10C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2385-10C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2301-10C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2301-10C>T
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8839
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2527
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 451
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 953
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18631
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8582
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1852
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 767
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24806
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2894
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum

19-55446039-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55446039
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55446039
    reference: chr 19
allele count: 1
allele frequency: 9.846590125839422e-6
allele num: 101558
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2217-12C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2301-12C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2385-12C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2217-12C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2301-12C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2301-12C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2301-12C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2301-12C>T
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 552
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9056
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20832
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7919
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13268
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2407
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 484
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27554
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1559
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum

19-55446041-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55446041
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55446041
    reference: chr 19
allele count: 2
allele frequency: 1.98609731876862e-5
allele num: 100700
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2301-14C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2385-14C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2301-14C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2301-14C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2301-14C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2217-14C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2217-14C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2301-14C>T
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21647
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 700
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2885
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12616
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 882
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 430
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 231
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1531
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 288
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28511
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

19-55446051-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55446051
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55446051
    reference: chr 19
allele count: 1
allele frequency: 1.053496555066265e-5
allele num: 94922
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2301-24T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2385-24T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2301-24T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2217-24T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2301-24T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2217-24T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2301-24T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2301-24T>C
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6857
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35365
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2837
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

19-55446070-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55446070
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55446070
    reference: chr 19
allele count: 5
allele frequency: 7.677896870489236e-5
allele num: 65122
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2301-43C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2385-43C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2301-43C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2301-43C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2217-43C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2301-43C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2301-43C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2217-43C>T
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1782
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20753
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7547
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20645
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24820
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 921
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2916
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13834
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

19-55446071-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55446071
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55446071
    reference: chr 19
allele count: 9
allele frequency: 1.446526728599441e-4
allele num: 62218
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2301-44A>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2301-44A>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2301-44A>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2385-44A>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2301-44A>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2217-44A>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2301-44A>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2217-44A>T
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 685
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21718
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6045
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7351
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19744
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 836
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 425
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1730
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5265
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3601
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14294
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: VQSLOD

19-55446072-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55446072
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55446072
    reference: chr 19
allele count: 2
allele frequency: 3.583073560500197e-5
allele num: 55818
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2301-45T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2217-45T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2385-45T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2301-45T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2217-45T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2301-45T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2301-45T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2301-45T>C
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6181
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6955
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18191
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23441
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6465
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1024
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19196
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5495
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 559
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum

19-55446075-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55446075
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55446075
    reference: chr 19
allele count: 1
allele frequency: 1.997124141236619e-5
allele num: 50072
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2217-48G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2385-48G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2301-48G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2301-48G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2217-48G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2301-48G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2301-48G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2301-48G>A
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17196
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6458
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24516
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6514
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1874
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14680
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7066
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2096
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 606
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16435
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3355
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

19-55447579-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447579
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447579
    reference: chr 19
allele count: 1
allele frequency: 8.329585020074299e-6
allele num: 120054
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+50G>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+50G>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+50G>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+50G>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+50G>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+50G>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+50G>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+50G>C
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13398
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1211
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3957
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum

19-55447579-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447579
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447579
    reference: chr 19
allele count: 1
allele frequency: 8.329585020074299e-6
allele num: 120054
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+50G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+50G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+50G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+50G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+50G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+50G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+50G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+50G>A
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8349
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6599
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2542
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6436
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1211
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1649
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1778
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: MQ

19-55447580-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447580
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447580
    reference: chr 19
allele count: 3
allele frequency: 2.499291867304264e-5
allele num: 120034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+49C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+49C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+49C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+49C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+49C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+49C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+49C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+49C>T
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13664
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4558
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11998
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8369
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3077
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14339
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3952
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-55447582-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447582
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447582
    reference: chr 19
allele count: 29
allele frequency: 2.413609428057793e-4
allele num: 120152
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+47A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+47A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+47A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+47A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+47A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+47A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+47A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+47A>G
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1609
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 501
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5574
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8378
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2784
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12544
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13757
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3116
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 588
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3947
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15058
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

19-55447589-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447589
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447589
    reference: chr 19
allele count: 21
allele frequency: 1.745781029179483e-4
allele num: 120290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+40C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+40C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+40C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+40C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+40C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+40C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+40C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+40C>T
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14115
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8597
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1468
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1092
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3144
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 753
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6638
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 511
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-55447589-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447589
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447589
    reference: chr 19
allele count: 7
allele frequency: 5.819270097264943e-5
allele num: 120290
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+40C>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+40C>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+40C>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+40C>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+40C>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+40C>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+40C>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+40C>G
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4600
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14115
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8597
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1606
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14415
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1663
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6638
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4029
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 886
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD

19-55447594-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447594
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447594
    reference: chr 19
allele count: 1
allele frequency: 8.312966565248474e-6
allele num: 120294
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+35G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+35G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+35G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+35G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+35G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+35G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+35G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+35G>A
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15317
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14421
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4633
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8828
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2197
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1607
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2138
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14401
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1289
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3165
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2262
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1692
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 4.25e1
  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: C
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ

19-55447595-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447595
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447595
    reference: chr 19
allele count: 27213
allele frequency: 2.262094763092269e-1
allele num: 120300
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+34T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+34T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+34T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+34T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+34T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+34T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+34T>C
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+34T>C
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 6.75e1
  variant carriers: 301
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.75e1
  variant carriers: 189
genotype depth: GenotypeDepth
  all individuals: 1104
  bin: 5.75e1
  variant carriers: 492
genotype depth: GenotypeDepth
  all individuals: 874
  bin: 6.25e1
  variant carriers: 348
genotype depth: GenotypeDepth
  all individuals: 9503
  bin: 3.25e1
  variant carriers: 3653
genotype depth: GenotypeDepth
  all individuals: 5950
  bin: 3.75e1
  variant carriers: 2904
genotype depth: GenotypeDepth
  all individuals: 11380
  bin: 2.25e1
  variant carriers: 2952
genotype depth: GenotypeDepth
  all individuals: 13755
  bin: 2.75e1
  variant carriers: 3838
genotype depth: GenotypeDepth
  all individuals: 2297
  bin: 4.75e1
  variant carriers: 1201
genotype depth: GenotypeDepth
  all individuals: 1377
  bin: 1.25e1
  variant carriers: 535
genotype depth: GenotypeDepth
  all individuals: 598
  bin: 7.75e1
  variant carriers: 208
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 7.25e1
  variant carriers: 253
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 75
genotype depth: GenotypeDepth
  all individuals: 2978
  bin: 9.75e1
  variant carriers: 2537
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 5.25e1
  variant carriers: 750
genotype depth: GenotypeDepth
  all individuals: 2569
  bin: 1.75e1
  variant carriers: 1690
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 9.25e1
  variant carriers: 131
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 8.25e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 3826
  bin: 4.25e1
  variant carriers: 2050
genotype quality: GenotypeQuality
  all individuals: 287
  bin: 2.75e1
  variant carriers: 52
genotype quality: GenotypeQuality
  all individuals: 620
  bin: 3.75e1
  variant carriers: 100
genotype quality: GenotypeQuality
  all individuals: 611
  bin: 4.75e1
  variant carriers: 168
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.75e1
  variant carriers: 42
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 3.25e1
  variant carriers: 106
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 1.25e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 2.25e1
  variant carriers: 64
genotype quality: GenotypeQuality
  all individuals: 1424
  bin: 9.25e1
  variant carriers: 197
num of homozygotes: 3130
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: A
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

19-55447599-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447599
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447598
    reference: chr 19
allele count: 1
allele frequency: 8.276090374906894e-6
allele num: 120830
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+29delG
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+29delG
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+29delG
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+29delG
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+29delG
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+29delG
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+29delG
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+29delG
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14128
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3712
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9506
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5830
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11726
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2244
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 842
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2924
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 953
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6158
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1027
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3430
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: GC
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-55447602-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447602
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447602
    reference: chr 19
allele count: 1
allele frequency: 8.275679433281473e-6
allele num: 120836
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+27C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+27C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+27C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+27C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+27C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+27C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+27C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+27C>T
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9560
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5834
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12050
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3714
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 643
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16996
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18229
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1772
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4009
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum

19-55447607-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447607
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447607
    reference: chr 19
allele count: 29
allele frequency: 2.39891469790219e-4
allele num: 120888
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+22C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+22C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+22C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+22C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+22C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+22C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+22C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+22C>T
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14409
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5848
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 860
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2250
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9612
  bin: 3.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 673
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2680
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3452
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17591
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

19-55447610-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447610
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447610
    reference: chr 19
allele count: 2
allele frequency: 1.654122901331569e-5
allele num: 120910
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+19G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+19G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+19G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+19G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+19G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+19G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+19G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+19G>A
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12452
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1109
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1323
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3716
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2246
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2689
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQ

19-55447612-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447612
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447612
    reference: chr 19
allele count: 13
allele frequency: 1.077300450808804e-4
allele num: 120672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+17C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+17C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+17C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+17C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+17C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+17C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+17C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+17C>T
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6166
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13331
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9269
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4504
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29553
  bin: 9.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 2026
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2140
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15063
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

19-55447612-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447612
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447612
    reference: chr 19
allele count: 25846
allele frequency: 2.141839034738796e-1
allele num: 120672
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+17C>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+17C>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+17C>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+17C>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+17C>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+17C>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+17C>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+17C>A
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.5e0
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 2184
  bin: 5.25e1
  variant carriers: 1375
genotype depth: GenotypeDepth
  all individuals: 3441
  bin: 9.75e1
  variant carriers: 2987
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 4.75e1
  variant carriers: 1935
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 6.75e1
  variant carriers: 361
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 5.75e1
  variant carriers: 918
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 1.75e1
  variant carriers: 755
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 1.25e1
  variant carriers: 238
genotype depth: GenotypeDepth
  all individuals: 6166
  bin: 3.75e1
  variant carriers: 2992
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 7.25e1
  variant carriers: 276
genotype depth: GenotypeDepth
  all individuals: 13331
  bin: 2.75e1
  variant carriers: 2578
genotype depth: GenotypeDepth
  all individuals: 10495
  bin: 2.25e1
  variant carriers: 1725
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.75e1
  variant carriers: 217
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 8.25e1
  variant carriers: 209
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 8.75e1
  variant carriers: 186
genotype depth: GenotypeDepth
  all individuals: 9269
  bin: 3.25e1
  variant carriers: 3049
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 6.25e1
  variant carriers: 584
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 9.25e1
  variant carriers: 159
genotype depth: GenotypeDepth
  all individuals: 4504
  bin: 4.25e1
  variant carriers: 2623
genotype quality: GenotypeQuality
  all individuals: 2499
  bin: 7.75e1
  variant carriers: 159
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 2.25e1
  variant carriers: 33
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.25e1
  variant carriers: 46
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 7.5e0
  variant carriers: 20
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 5.25e1
  variant carriers: 110
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 4.75e1
  variant carriers: 79
genotype quality: GenotypeQuality
  all individuals: 228
  bin: 5.75e1
  variant carriers: 91
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 34
num of homozygotes: 2792
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum

19-55447617-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447617
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447617
    reference: chr 19
allele count: 140
allele frequency: 1.1562985232416e-3
allele num: 121076
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+12G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+12G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+12G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+12G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+12G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+12G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+12G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+12G>A
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16426
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3667
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 9.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 9885
  bin: 3.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11724
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 7.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 3205
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2272
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3939
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 1
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD

19-55447618-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447618
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447618
    reference: chr 19
allele count: 8
allele frequency: 6.606656206127674e-5
allele num: 121090
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+11C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+11C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+11C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+11C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+11C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+11C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+11C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+11C>T
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 709
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11754
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7177
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21303
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

19-55447626-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447626
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447626
    reference: chr 19
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2300+3G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2216+3G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2216+3G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2384+3G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2300+3G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2300+3G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2300+3G>A
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2300+3G>A
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1030
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9946
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16664
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3134
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7227
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: c.2300+3G>A
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

19-55447630-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447630
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447630
    reference: chr 19
allele count: 1
allele frequency: 8.251642076773278e-6
allele num: 121188
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2299A>G
  hgvsp: ENSP00000468706.1:p.Arg767Gly
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2299A>G
  hgvsp: ENSP00000468243.1:p.Arg767Gly
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2299A>G
  hgvsp: ENSP00000339491.2:p.Arg767Gly
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2299A>G
  hgvsp: ENSP00000467123.1:p.Arg767Gly
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2383A>G
  hgvsp: ENSP00000414273.1:p.Arg795Gly
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2299A>G
  hgvsp: ENSP00000465520.1:p.Arg767Gly
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2215A>G
  hgvsp: ENSP00000409137.2:p.Arg739Gly
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2215A>G
  hgvsp: ENSP00000329568.5:p.Arg739Gly
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9948
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2458
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5585
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16729
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21894
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3234
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Arg767Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

19-55447644-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447644
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447644
    reference: chr 19
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2369A>T
  hgvsp: ENSP00000414273.1:p.Asn790Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2285A>T
  hgvsp: ENSP00000339491.2:p.Asn762Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2285A>T
  hgvsp: ENSP00000465520.1:p.Asn762Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2285A>T
  hgvsp: ENSP00000468706.1:p.Asn762Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2201A>T
  hgvsp: ENSP00000329568.5:p.Asn734Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2285A>T
  hgvsp: ENSP00000468243.1:p.Asn762Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2201A>T
  hgvsp: ENSP00000409137.2:p.Asn734Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2285A>T
  hgvsp: ENSP00000467123.1:p.Asn762Ile
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11834
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10005
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16890
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3233
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn762Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

19-55447646-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447646
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447646
    reference: chr 19
allele count: 5
allele frequency: 4.124595789612618e-5
allele num: 121224
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2283C>T
  hgvsp: ENST00000588756.1:c.2283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2199C>T
  hgvsp: ENST00000328092.5:c.2199C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2283C>T
  hgvsp: ENST00000340844.2:c.2283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2283C>T
  hgvsp: ENST00000586379.1:c.2283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2283C>T
  hgvsp: ENST00000590030.1:c.2283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2367C>T
  hgvsp: ENST00000446217.1:c.2367C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2283C>T
  hgvsp: ENST00000592784.1:c.2283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2199C>T
  hgvsp: ENST00000448121.2:c.2199C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10024
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5604
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11809
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16911
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7234
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21930
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Cys761Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

19-55447659-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447659
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447659
    reference: chr 19
allele count: 3
allele frequency: 2.474104374216534e-5
allele num: 121256
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2270G>C
  hgvsp: ENSP00000468243.1:p.Arg757Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2354G>C
  hgvsp: ENSP00000414273.1:p.Arg785Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2186G>C
  hgvsp: ENSP00000409137.2:p.Arg729Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2270G>C
  hgvsp: ENSP00000465520.1:p.Arg757Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2270G>C
  hgvsp: ENSP00000467123.1:p.Arg757Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2270G>C
  hgvsp: ENSP00000468706.1:p.Arg757Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2270G>C
  hgvsp: ENSP00000339491.2:p.Arg757Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2186G>C
  hgvsp: ENSP00000329568.5:p.Arg729Thr
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10051
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11817
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22027
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 184
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg757Thr
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP

19-55447675-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447675
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447675
    reference: chr 19
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2254C>G
  hgvsp: ENSP00000339491.2:p.Leu752Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2170C>G
  hgvsp: ENSP00000409137.2:p.Leu724Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2338C>G
  hgvsp: ENSP00000414273.1:p.Leu780Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2254C>G
  hgvsp: ENSP00000465520.1:p.Leu752Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2254C>G
  hgvsp: ENSP00000467123.1:p.Leu752Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2170C>G
  hgvsp: ENSP00000329568.5:p.Leu724Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2254C>G
  hgvsp: ENSP00000468243.1:p.Leu752Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2254C>G
  hgvsp: ENSP00000468706.1:p.Leu752Val
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10101
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11524
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2254
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1655
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16173
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Leu752Val
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

19-55447681-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447681
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447681
    reference: chr 19
allele count: 58
allele frequency: 4.783347353489369e-4
allele num: 121254
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2248C>G
  hgvsp: ENSP00000468706.1:p.Leu750Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2248C>G
  hgvsp: ENSP00000468243.1:p.Leu750Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2248C>G
  hgvsp: ENSP00000339491.2:p.Leu750Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2164C>G
  hgvsp: ENSP00000329568.5:p.Leu722Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2164C>G
  hgvsp: ENSP00000409137.2:p.Leu722Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2332C>G
  hgvsp: ENSP00000414273.1:p.Leu778Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2248C>G
  hgvsp: ENSP00000465520.1:p.Leu750Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2248C>G
  hgvsp: ENSP00000467123.1:p.Leu750Val
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 11388
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17167
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 5.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5610
  bin: 3.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10076
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3681
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16224
  bin: 9.75e1
  variant carriers: 58
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 295
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu750Val
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

19-55447688-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447688
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447688
    reference: chr 19
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2157G>C
  hgvsp: ENST00000448121.2:c.2157G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2241G>C
  hgvsp: ENST00000586379.1:c.2241G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2241G>C
  hgvsp: ENST00000592784.1:c.2241G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2241G>C
  hgvsp: ENST00000588756.1:c.2241G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2325G>C
  hgvsp: ENST00000446217.1:c.2325G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2157G>C
  hgvsp: ENST00000328092.5:c.2157G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2241G>C
  hgvsp: ENST00000340844.2:c.2241G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2241G>C
  hgvsp: ENST00000590030.1:c.2241G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11436
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10063
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1034
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2251
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1649
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21660
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16166
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Thr747Thr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum

19-55447689-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447689
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447689
    reference: chr 19
allele count: 7
allele frequency: 5.772814989526464e-5
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2156C>T
  hgvsp: ENSP00000409137.2:p.Thr719Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2240C>T
  hgvsp: ENSP00000339491.2:p.Thr747Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2240C>T
  hgvsp: ENSP00000468243.1:p.Thr747Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2240C>T
  hgvsp: ENSP00000468706.1:p.Thr747Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2240C>T
  hgvsp: ENSP00000467123.1:p.Thr747Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2324C>T
  hgvsp: ENSP00000414273.1:p.Thr775Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2240C>T
  hgvsp: ENSP00000465520.1:p.Thr747Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2156C>T
  hgvsp: ENSP00000329568.5:p.Thr719Met
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5588
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 689
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10046
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17201
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7133
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2252
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr747Met
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: MQ

19-55447693-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447693
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447693
    reference: chr 19
allele count: 28
allele frequency: 2.309392629738379e-4
allele num: 121244
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2236C>T
  hgvsp: ENSP00000467123.1:p.Arg746Cys
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2236C>T
  hgvsp: ENSP00000339491.2:p.Arg746Cys
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2236C>T
  hgvsp: ENSP00000468243.1:p.Arg746Cys
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2236C>T
  hgvsp: ENSP00000468706.1:p.Arg746Cys
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2152C>T
  hgvsp: ENSP00000409137.2:p.Arg718Cys
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2152C>T
  hgvsp: ENSP00000329568.5:p.Arg718Cys
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2236C>T
  hgvsp: ENSP00000465520.1:p.Arg746Cys
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2320C>T
  hgvsp: ENSP00000414273.1:p.Arg774Cys
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1499
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17232
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11408
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 10029
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 186
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1651
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg746Cys
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD

19-55447700-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447700
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447700
    reference: chr 19
allele count: 6
allele frequency: 4.947474314362518e-5
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2229G>A
  hgvsp: ENST00000340844.2:c.2229G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2229G>A
  hgvsp: ENST00000592784.1:c.2229G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2229G>A
  hgvsp: ENST00000588756.1:c.2229G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2229G>A
  hgvsp: ENST00000586379.1:c.2229G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2145G>A
  hgvsp: ENST00000328092.5:c.2145G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2145G>A
  hgvsp: ENST00000448121.2:c.2145G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2313G>A
  hgvsp: ENST00000446217.1:c.2313G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2229G>A
  hgvsp: ENST00000590030.1:c.2229G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11471
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5587
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1035
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17273
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3816
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu743Glu
num of homozygotes: 1
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

19-55447702-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447702
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447702
    reference: chr 19
allele count: 3
allele frequency: 2.473941153186436e-5
allele num: 121264
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2311G>A
  hgvsp: ENSP00000414273.1:p.Glu771Lys
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2227G>A
  hgvsp: ENSP00000468706.1:p.Glu743Lys
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2227G>A
  hgvsp: ENSP00000339491.2:p.Glu743Lys
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2143G>A
  hgvsp: ENSP00000409137.2:p.Glu715Lys
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2227G>A
  hgvsp: ENSP00000468243.1:p.Glu743Lys
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2143G>A
  hgvsp: ENSP00000329568.5:p.Glu715Lys
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2227G>A
  hgvsp: ENSP00000467123.1:p.Glu743Lys
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2227G>A
  hgvsp: ENSP00000465520.1:p.Glu743Lys
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3673
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 782
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17277
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10013
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 168
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3809
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu743Lys
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: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-55447703-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447703
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447703
    reference: chr 19
allele count: 14
allele frequency: 1.154429711722409e-4
allele num: 121272
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2226C>T
  hgvsp: ENST00000586379.1:c.2226C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2226C>T
  hgvsp: ENST00000340844.2:c.2226C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2226C>T
  hgvsp: ENST00000588756.1:c.2226C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2226C>T
  hgvsp: ENST00000590030.1:c.2226C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2310C>T
  hgvsp: ENST00000446217.1:c.2310C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2142C>T
  hgvsp: ENST00000448121.2:c.2142C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2142C>T
  hgvsp: ENST00000328092.5:c.2142C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2226C>T
  hgvsp: ENST00000592784.1:c.2226C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11518
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 9994
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5591
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 692
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17263
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22059
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7124
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile742Ile
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-55447708-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447708
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447708
    reference: chr 19
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2137C>T
  hgvsp: ENSP00000409137.2:p.His713Tyr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2305C>T
  hgvsp: ENSP00000414273.1:p.His769Tyr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2221C>T
  hgvsp: ENSP00000468243.1:p.His741Tyr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2221C>T
  hgvsp: ENSP00000467123.1:p.His741Tyr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2137C>T
  hgvsp: ENSP00000329568.5:p.His713Tyr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2221C>T
  hgvsp: ENSP00000339491.2:p.His741Tyr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2221C>T
  hgvsp: ENSP00000468706.1:p.His741Tyr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2221C>T
  hgvsp: ENSP00000465520.1:p.His741Tyr
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9979
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17313
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3674
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16172
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22191
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 5.25e1
  variant carriers: 0
hgvs: p.His741Tyr
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

19-55447710-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447710
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447710
    reference: chr 19
allele count: 2
allele frequency: 1.649130908011478e-5
allele num: 121276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2219G>A
  hgvsp: ENSP00000465520.1:p.Gly740Glu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2219G>A
  hgvsp: ENSP00000468706.1:p.Gly740Glu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2135G>A
  hgvsp: ENSP00000329568.5:p.Gly712Glu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2303G>A
  hgvsp: ENSP00000414273.1:p.Gly768Glu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2135G>A
  hgvsp: ENSP00000409137.2:p.Gly712Glu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2219G>A
  hgvsp: ENSP00000467123.1:p.Gly740Glu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2219G>A
  hgvsp: ENSP00000339491.2:p.Gly740Glu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2219G>A
  hgvsp: ENSP00000468243.1:p.Gly740Glu
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3671
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1266
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 784
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1487
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16171
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3111
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly740Glu
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

19-55447717-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447717
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447717
    reference: chr 19
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2212C>A
  hgvsp: ENSP00000468243.1:p.Leu738Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2212C>A
  hgvsp: ENSP00000339491.2:p.Leu738Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2212C>A
  hgvsp: ENSP00000468706.1:p.Leu738Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2212C>A
  hgvsp: ENSP00000465520.1:p.Leu738Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2128C>A
  hgvsp: ENSP00000409137.2:p.Leu710Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2296C>A
  hgvsp: ENSP00000414273.1:p.Leu766Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2212C>A
  hgvsp: ENSP00000467123.1:p.Leu738Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2128C>A
  hgvsp: ENSP00000329568.5:p.Leu710Met
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5581
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2252
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7129
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu738Met
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

19-55447719-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447719
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447719
    reference: chr 19
allele count: 2
allele frequency: 1.648994937585542e-5
allele num: 121286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2210C>T
  hgvsp: ENSP00000468243.1:p.Thr737Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2210C>T
  hgvsp: ENSP00000468706.1:p.Thr737Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2294C>T
  hgvsp: ENSP00000414273.1:p.Thr765Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2126C>T
  hgvsp: ENSP00000329568.5:p.Thr709Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2210C>T
  hgvsp: ENSP00000339491.2:p.Thr737Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2126C>T
  hgvsp: ENSP00000409137.2:p.Thr709Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2210C>T
  hgvsp: ENSP00000467123.1:p.Thr737Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2210C>T
  hgvsp: ENSP00000465520.1:p.Thr737Ile
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17445
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9950
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2467
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16171
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 150
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3102
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr737Ile
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

19-55447727-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447727
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447727
    reference: chr 19
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2202G>A
  hgvsp: ENST00000340844.2:c.2202G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2202G>A
  hgvsp: ENST00000588756.1:c.2202G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2202G>A
  hgvsp: ENST00000586379.1:c.2202G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2202G>A
  hgvsp: ENST00000592784.1:c.2202G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2286G>A
  hgvsp: ENST00000446217.1:c.2286G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2202G>A
  hgvsp: ENST00000590030.1:c.2202G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2118G>A
  hgvsp: ENST00000448121.2:c.2118G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2118G>A
  hgvsp: ENST00000328092.5:c.2118G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1485
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2250
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7072
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr734Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

19-55447728-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447728
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447728
    reference: chr 19
allele count: 100
allele frequency: 8.244974687927708e-4
allele num: 121286
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2201C>T
  hgvsp: ENSP00000339491.2:p.Thr734Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2201C>T
  hgvsp: ENSP00000468243.1:p.Thr734Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2285C>T
  hgvsp: ENSP00000414273.1:p.Thr762Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2201C>T
  hgvsp: ENSP00000468706.1:p.Thr734Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2201C>T
  hgvsp: ENSP00000467123.1:p.Thr734Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2201C>T
  hgvsp: ENSP00000465520.1:p.Thr734Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2117C>T
  hgvsp: ENSP00000409137.2:p.Thr706Met
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2117C>T
  hgvsp: ENSP00000329568.5:p.Thr706Met
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5577
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11629
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3665
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 9.75e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9951
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1673
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17470
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 6.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3088
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr734Met
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

19-55447730-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447730
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447730
    reference: chr 19
allele count: 4
allele frequency: 3.29777235477435e-5
allele num: 121294
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2199C>T
  hgvsp: ENST00000592784.1:c.2199C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2199C>T
  hgvsp: ENST00000588756.1:c.2199C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2199C>T
  hgvsp: ENST00000340844.2:c.2199C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2283C>T
  hgvsp: ENST00000446217.1:c.2283C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2199C>T
  hgvsp: ENST00000590030.1:c.2199C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2115C>T
  hgvsp: ENST00000448121.2:c.2115C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2199C>T
  hgvsp: ENST00000586379.1:c.2199C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2115C>T
  hgvsp: ENST00000328092.5:c.2115C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9945
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17482
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3662
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1649
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22883
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu733Leu
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-55447732-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447732
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447732
    reference: chr 19
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2197C>T
  hgvsp: ENSP00000468243.1:p.Leu733Phe
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2197C>T
  hgvsp: ENSP00000465520.1:p.Leu733Phe
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2281C>T
  hgvsp: ENSP00000414273.1:p.Leu761Phe
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2113C>T
  hgvsp: ENSP00000329568.5:p.Leu705Phe
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2197C>T
  hgvsp: ENSP00000339491.2:p.Leu733Phe
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2197C>T
  hgvsp: ENSP00000468706.1:p.Leu733Phe
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2113C>T
  hgvsp: ENSP00000409137.2:p.Leu705Phe
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2197C>T
  hgvsp: ENSP00000467123.1:p.Leu733Phe
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9940
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11680
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2253
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1650
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu733Phe
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

19-55447745-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447745
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447745
    reference: chr 19
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2184T>C
  hgvsp: ENST00000592784.1:c.2184T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2184T>C
  hgvsp: ENST00000340844.2:c.2184T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2184T>C
  hgvsp: ENST00000588756.1:c.2184T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2268T>C
  hgvsp: ENST00000446217.1:c.2268T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2100T>C
  hgvsp: ENST00000448121.2:c.2100T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2184T>C
  hgvsp: ENST00000590030.1:c.2184T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2184T>C
  hgvsp: ENST00000586379.1:c.2184T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2100T>C
  hgvsp: ENST00000328092.5:c.2100T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17540
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3660
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5562
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2466
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7066
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile728Ile
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/19-55447767-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447767
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447767
    reference: chr 19
allele count: 3
allele frequency: 2.476309967973058e-5
allele num: 121148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2162G>T
  hgvsp: ENSP00000339491.2:p.Arg721Leu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2162G>T
  hgvsp: ENSP00000468706.1:p.Arg721Leu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2078G>T
  hgvsp: ENSP00000329568.5:p.Arg693Leu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2246G>T
  hgvsp: ENSP00000414273.1:p.Arg749Leu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2162G>T
  hgvsp: ENSP00000468243.1:p.Arg721Leu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2162G>T
  hgvsp: ENSP00000467123.1:p.Arg721Leu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2078G>T
  hgvsp: ENSP00000409137.2:p.Arg693Leu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2162G>T
  hgvsp: ENSP00000465520.1:p.Arg721Leu
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11569
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1045
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17473
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5572
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1648
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg721Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS

19-55447768-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447768
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447768
    reference: chr 19
allele count: 4
allele frequency: 3.301910155024682e-5
allele num: 121142
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2161C>T
  hgvsp: ENSP00000339491.2:p.Arg721Trp
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2161C>T
  hgvsp: ENSP00000467123.1:p.Arg721Trp
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2161C>T
  hgvsp: ENSP00000468243.1:p.Arg721Trp
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2245C>T
  hgvsp: ENSP00000414273.1:p.Arg749Trp
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2161C>T
  hgvsp: ENSP00000468706.1:p.Arg721Trp
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2077C>T
  hgvsp: ENSP00000329568.5:p.Arg693Trp
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2077C>T
  hgvsp: ENSP00000409137.2:p.Arg693Trp
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2161C>T
  hgvsp: ENSP00000465520.1:p.Arg721Trp
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9875
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3083
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1649
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3730
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg721Trp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD

19-55447772-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447772
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447772
    reference: chr 19
allele count: 15
allele frequency: 1.238543472875898e-4
allele num: 121110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2157G>A
  hgvsp: ENST00000586379.1:c.2157G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2073G>A
  hgvsp: ENST00000328092.5:c.2073G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2241G>A
  hgvsp: ENST00000446217.1:c.2241G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2157G>A
  hgvsp: ENST00000590030.1:c.2157G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2073G>A
  hgvsp: ENST00000448121.2:c.2073G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2157G>A
  hgvsp: ENST00000340844.2:c.2157G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2157G>A
  hgvsp: ENST00000588756.1:c.2157G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2157G>A
  hgvsp: ENST00000592784.1:c.2157G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17438
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11546
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5559
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2472
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3086
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3048
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala719Ala
num of homozygotes: 1
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

19-55447773-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447773
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447773
    reference: chr 19
allele count: 144
allele frequency: 1.189296333002973e-3
allele num: 121080
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2156C>T
  hgvsp: ENSP00000468243.1:p.Ala719Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2240C>T
  hgvsp: ENSP00000414273.1:p.Ala747Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2156C>T
  hgvsp: ENSP00000339491.2:p.Ala719Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2156C>T
  hgvsp: ENSP00000467123.1:p.Ala719Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2072C>T
  hgvsp: ENSP00000329568.5:p.Ala691Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2072C>T
  hgvsp: ENSP00000409137.2:p.Ala691Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2156C>T
  hgvsp: ENSP00000468706.1:p.Ala719Val
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2156C>T
  hgvsp: ENSP00000465520.1:p.Ala719Val
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5553
  bin: 3.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 9821
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 6.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 4.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1053
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 17392
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 7.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 4.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11516
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1689
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1488
  bin: 9.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 7.25e1
  variant carriers: 17
genotype quality: GenotypeQuality
  all individuals: 1636
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3073
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16254
  bin: 9.75e1
  variant carriers: 144
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala719Val
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-55447774-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447774
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447774
    reference: chr 19
allele count: 9
allele frequency: 7.432979303282074e-5
allele num: 121082
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2155G>A
  hgvsp: ENSP00000468243.1:p.Ala719Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2155G>A
  hgvsp: ENSP00000467123.1:p.Ala719Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2155G>A
  hgvsp: ENSP00000339491.2:p.Ala719Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2071G>A
  hgvsp: ENSP00000409137.2:p.Ala691Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2155G>A
  hgvsp: ENSP00000465520.1:p.Ala719Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2071G>A
  hgvsp: ENSP00000329568.5:p.Ala691Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2155G>A
  hgvsp: ENSP00000468706.1:p.Ala719Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2239G>A
  hgvsp: ENSP00000414273.1:p.Ala747Thr
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17416
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11517
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3660
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2248
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3078
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala719Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

19-55447775-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447775
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447775
    reference: chr 19
allele count: 8
allele frequency: 6.610040651750008e-5
allele num: 121028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2154C>T
  hgvsp: ENST00000590030.1:c.2154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2154C>T
  hgvsp: ENST00000586379.1:c.2154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2070C>T
  hgvsp: ENST00000328092.5:c.2070C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2154C>T
  hgvsp: ENST00000592784.1:c.2154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2154C>T
  hgvsp: ENST00000340844.2:c.2154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2154C>T
  hgvsp: ENST00000588756.1:c.2154C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2238C>T
  hgvsp: ENST00000446217.1:c.2238C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2070C>T
  hgvsp: ENST00000448121.2:c.2070C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5566
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11460
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3660
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2468
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17376
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3718
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3028
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2244
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr718Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum

19-55447781-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447781
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447781
    reference: chr 19
allele count: 2
allele frequency: 1.653220473482343e-5
allele num: 120976
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2232T>C
  hgvsp: ENST00000446217.1:c.2232T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2064T>C
  hgvsp: ENST00000328092.5:c.2064T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2148T>C
  hgvsp: ENST00000586379.1:c.2148T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2148T>C
  hgvsp: ENST00000592784.1:c.2148T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2148T>C
  hgvsp: ENST00000340844.2:c.2148T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2148T>C
  hgvsp: ENST00000590030.1:c.2148T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2148T>C
  hgvsp: ENST00000588756.1:c.2148T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2064T>C
  hgvsp: ENST00000448121.2:c.2064T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro716Pro
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD

19-55447781-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447781
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447781
    reference: chr 19
allele count: 1
allele frequency: 8.266102367411717e-6
allele num: 120976
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2064T>A
  hgvsp: ENST00000328092.5:c.2064T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2148T>A
  hgvsp: ENST00000588756.1:c.2148T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2232T>A
  hgvsp: ENST00000446217.1:c.2232T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2148T>A
  hgvsp: ENST00000340844.2:c.2148T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2148T>A
  hgvsp: ENST00000592784.1:c.2148T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2148T>A
  hgvsp: ENST00000590030.1:c.2148T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2148T>A
  hgvsp: ENST00000586379.1:c.2148T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2064T>A
  hgvsp: ENST00000448121.2:c.2064T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9809
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17320
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 205
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22684
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3020
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Pro716Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: A
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

19-55447781-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447781
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447780
    reference: chr 19
allele count: 2
allele frequency: 1.653220473482343e-5
allele num: 120976
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2063delC
  hgvsp: ENSP00000409137.2:p.Pro688LeufsTer21
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2147delC
  hgvsp: ENSP00000465520.1:p.Pro716LeufsTer21
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2147delC
  hgvsp: ENSP00000339491.2:p.Pro716LeufsTer21
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2147delC
  hgvsp: ENSP00000467123.1:p.Pro716LeufsTer21
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2063delC
  hgvsp: ENSP00000329568.5:p.Pro688LeufsTer21
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2147delC
  hgvsp: ENSP00000468706.1:p.Pro716LeufsTer21
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2147delC
  hgvsp: ENSP00000468243.1:p.Pro716LeufsTer21
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2231delC
  hgvsp: ENSP00000414273.1:p.Pro744LeufsTer21
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2469
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11503
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9809
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16154
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro716LeufsTer21
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: AG
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

19-55447782-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447782
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447782
    reference: chr 19
allele count: 1
allele frequency: 8.266375690242371e-6
allele num: 120972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2147C>T
  hgvsp: ENSP00000468706.1:p.Pro716Leu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2147C>T
  hgvsp: ENSP00000339491.2:p.Pro716Leu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2147C>T
  hgvsp: ENSP00000468243.1:p.Pro716Leu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2231C>T
  hgvsp: ENSP00000414273.1:p.Pro744Leu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2147C>T
  hgvsp: ENSP00000465520.1:p.Pro716Leu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2147C>T
  hgvsp: ENSP00000467123.1:p.Pro716Leu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2063C>T
  hgvsp: ENSP00000409137.2:p.Pro688Leu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2063C>T
  hgvsp: ENSP00000329568.5:p.Pro688Leu
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17304
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3702
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16154
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro716Leu
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP

19-55447783-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447783
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447783
    reference: chr 19
allele count: 6
allele frequency: 4.95998941868924e-5
allele num: 120968
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2146C>G
  hgvsp: ENSP00000468706.1:p.Pro716Ala
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2146C>G
  hgvsp: ENSP00000467123.1:p.Pro716Ala
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2230C>G
  hgvsp: ENSP00000414273.1:p.Pro744Ala
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2062C>G
  hgvsp: ENSP00000409137.2:p.Pro688Ala
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2146C>G
  hgvsp: ENSP00000339491.2:p.Pro716Ala
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2062C>G
  hgvsp: ENSP00000329568.5:p.Pro688Ala
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2146C>G
  hgvsp: ENSP00000468243.1:p.Pro716Ala
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2146C>G
  hgvsp: ENSP00000465520.1:p.Pro716Ala
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3656
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 698
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11543
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1681
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17293
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 127
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2241
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro716Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
reference allele: G
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

19-55447789-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447789
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447789
    reference: chr 19
allele count: 6
allele frequency: 4.96310756708467e-5
allele num: 120892
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2140G>A
  hgvsp: ENSP00000468243.1:p.Val714Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2140G>A
  hgvsp: ENSP00000467123.1:p.Val714Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2140G>A
  hgvsp: ENSP00000468706.1:p.Val714Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2224G>A
  hgvsp: ENSP00000414273.1:p.Val742Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2140G>A
  hgvsp: ENSP00000465520.1:p.Val714Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2056G>A
  hgvsp: ENSP00000409137.2:p.Val686Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2140G>A
  hgvsp: ENSP00000339491.2:p.Val714Ile
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2056G>A
  hgvsp: ENSP00000329568.5:p.Val686Ile
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9747
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11476
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3659
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17177
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5539
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1682
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3689
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Val714Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

19-55447790-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447790
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447790
    reference: chr 19
allele count: 4
allele frequency: 3.308683640213741e-5
allele num: 120894
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2055C>T
  hgvsp: ENST00000448121.2:c.2055C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2139C>T
  hgvsp: ENST00000590030.1:c.2139C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2223C>T
  hgvsp: ENST00000446217.1:c.2223C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2139C>T
  hgvsp: ENST00000586379.1:c.2139C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2055C>T
  hgvsp: ENST00000328092.5:c.2055C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2139C>T
  hgvsp: ENST00000588756.1:c.2139C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2139C>T
  hgvsp: ENST00000592784.1:c.2139C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2139C>T
  hgvsp: ENST00000340844.2:c.2139C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3661
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11487
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9743
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 626
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1052
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5547
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3056
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1638
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn713Asn
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

19-55447794-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447794
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447794
    reference: chr 19
allele count: 1
allele frequency: 8.274309922552459e-6
allele num: 120856
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2219A>C
  hgvsp: ENSP00000414273.1:p.Lys740Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2135A>C
  hgvsp: ENSP00000339491.2:p.Lys712Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2135A>C
  hgvsp: ENSP00000468706.1:p.Lys712Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2135A>C
  hgvsp: ENSP00000465520.1:p.Lys712Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2051A>C
  hgvsp: ENSP00000409137.2:p.Lys684Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2135A>C
  hgvsp: ENSP00000468243.1:p.Lys712Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2135A>C
  hgvsp: ENSP00000467123.1:p.Lys712Thr
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2051A>C
  hgvsp: ENSP00000329568.5:p.Lys684Thr
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11428
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1272
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22499
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2998
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 282
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Lys712Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

19-55447795-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447795
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447795
    reference: chr 19
allele count: 14
allele frequency: 1.158556769281695e-4
allele num: 120840
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2050A>G
  hgvsp: ENSP00000329568.5:p.Lys684Glu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2134A>G
  hgvsp: ENSP00000468243.1:p.Lys712Glu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2134A>G
  hgvsp: ENSP00000465520.1:p.Lys712Glu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2134A>G
  hgvsp: ENSP00000468706.1:p.Lys712Glu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2134A>G
  hgvsp: ENSP00000467123.1:p.Lys712Glu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2134A>G
  hgvsp: ENSP00000339491.2:p.Lys712Glu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2050A>G
  hgvsp: ENSP00000409137.2:p.Lys684Glu
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2218A>G
  hgvsp: ENSP00000414273.1:p.Lys740Glu
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17064
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9692
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2461
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 200
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22417
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys712Glu
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

19-55447801-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447801
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447801
    reference: chr 19
allele count: 1
allele frequency: 8.281985026171072e-6
allele num: 120744
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2130-2A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2046-2A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2130-2A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2046-2A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2130-2A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2214-2A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2130-2A>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2130-2A>G
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9643
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11267
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 894
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16151
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 374
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 751
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
hgvs: c.2130-2A>G
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

19-55447804-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447804
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447804
    reference: chr 19
allele count: 1
allele frequency: 8.284043275842073e-6
allele num: 120714
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2130-5C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2214-5C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2130-5C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2046-5C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2130-5C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2130-5C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2046-5C>T
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2130-5C>T
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9620
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16835
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2463
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11205
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5524
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6681
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16154
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3647
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
hgvs: c.2130-5C>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/19-55447809-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447809
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447809
    reference: chr 19
allele count: 1
allele frequency: 8.288162845823595e-6
allele num: 120654
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2046-10T>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2214-10T>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2130-10T>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2130-10T>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2130-10T>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2130-10T>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2046-10T>G
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2130-10T>G
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1345
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10956
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2942
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 534
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 352
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

19-55447821-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 55447821
    reference: chr 19
  end: Position
    type: ExactPosition
    position: 55447822
    reference: chr 19
allele count: 1
allele frequency: 8.300959590928711e-6
allele num: 120468
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000409137
  ensembl transcript: ENST00000448121
  gene symbol: NLRP7
  hgvsc: ENST00000448121.2:c.2046-23dupG
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000329568
  ensembl transcript: ENST00000328092
  gene symbol: NLRP7
  hgvsc: ENST00000328092.5:c.2046-23dupG
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468243
  ensembl transcript: ENST00000586379
  gene symbol: NLRP7
  hgvsc: ENST00000586379.1:c.2130-23dupG
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000468706
  ensembl transcript: ENST00000592784
  gene symbol: NLRP7
  hgvsc: ENST00000592784.1:c.2130-23dupG
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000339491
  ensembl transcript: ENST00000340844
  gene symbol: NLRP7
  hgvsc: ENST00000340844.2:c.2130-23dupG
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000467123
  ensembl transcript: ENST00000588756
  gene symbol: NLRP7
  hgvsc: ENST00000588756.1:c.2130-23dupG
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000414273
  ensembl transcript: ENST00000446217
  gene symbol: NLRP7
  hgvsc: ENST00000446217.1:c.2214-23dupG
  variant of: http://identifiers.org/hgnc/22947
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000167634
  ensembl protein: ENSP00000465520
  ensembl transcript: ENST00000590030
  gene symbol: NLRP7
  hgvsc: ENST00000590030.1:c.2130-23dupG
  variant of: http://identifiers.org/hgnc/22947
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1051
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1680
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9363
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1271
  bin: 5.75e1
  variant carriers: 1
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 244
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1009
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16062
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 611
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33090
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1122
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4744
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 9.75e1
variant carriers: 6

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5990
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9552
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 806
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 7.85751702462022e-4
allele num: 7636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 59670
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 9.52e0

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

DP
type: SiteQuality
SIO_000300: 1.351566e6

VQSLOD
type: SiteQuality
SIO_000300: 1.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.738e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.7e-2

FS
type: SiteQuality
SIO_000300: 1.025e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.1e-3

GenotypeQuality
all individuals: 1050
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 623
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4639
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 268
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 810
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5964
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15108
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.686511282760482e-5
allele num: 59294
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9510
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.331616e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.49e-1

MQ
type: SiteQuality
SIO_000300: 5.928e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.51e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

QD
type: SiteQuality
SIO_000300: 1.446e1

VQSLOD
type: SiteQuality
SIO_000300: 3.06e0

GenotypeQuality
all individuals: 270
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1210
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 222
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 529
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20876
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 671
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28406
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5858
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.098901098901099e-4
allele num: 9100
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14874
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58072
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.447e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.037e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.52e-1

QD
type: SiteQuality
SIO_000300: 3.98e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

DP
type: SiteQuality
SIO_000300: 1.257563e6

GenotypeQuality
all individuals: 1234
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 647
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3772
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21726
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1573
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 594
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 94
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5820
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9032
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57714
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.347164219318335e-4
allele num: 14846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7312
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9296
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 782
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.82e0

MQ
type: SiteQuality
SIO_000300: 6.063e1

MQRankSum
type: SiteQuality
SIO_000300: 5.92e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.01e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

QD
type: SiteQuality
SIO_000300: 8.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.54e-1

DP
type: SiteQuality
SIO_000300: 1.240152e6

GenotypeQuality
all individuals: 677
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 357
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27993
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 518
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1571
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 1.073652566029633e-4
allele num: 9314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57720
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14828
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9014
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7318
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5822
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 784
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

VQSLOD
type: SiteQuality
SIO_000300: 6.99e-1

DP
type: SiteQuality
SIO_000300: 1.237757e6

FS
type: SiteQuality
SIO_000300: 4.428e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.05e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.67e-1

QD
type: SiteQuality
SIO_000300: 1.64e1

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
all individuals: 24943
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 788
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 291
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1459
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 821
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8842
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 766
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5712
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7160
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14704
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.521746786406058e-5
allele num: 56790
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.928e1

MQRankSum
type: SiteQuality
SIO_000300: 4.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.69e0

QD
type: SiteQuality
SIO_000300: 1.534e1

VQSLOD
type: SiteQuality
SIO_000300: -1.211e0

DP
type: SiteQuality
SIO_000300: 1.176465e6

FS
type: SiteQuality
SIO_000300: 1.1004e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -8.39e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.54e-1

GenotypeQuality
all individuals: 95
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 363
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1400
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25127
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 203
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9172
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14666
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.133529811834051e-4
allele num: 8822
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5706
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56640
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 762
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.74e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.09e0

FS
type: SiteQuality
SIO_000300: 2.037e0

DP
type: SiteQuality
SIO_000300: 1.172493e6

QD
type: SiteQuality
SIO_000300: 8.640000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e0

GenotypeQuality
all individuals: 270
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9078
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7028
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5624
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 748
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8674
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55872
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.88041832943443e-5
allele num: 14534
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.61e-1

FS
type: SiteQuality
SIO_000300: 6.443e0

MQRankSum
type: SiteQuality
SIO_000300: 1.12e0

DP
type: SiteQuality
SIO_000300: 1.124596e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

MQ
type: SiteQuality
SIO_000300: 5.933e1

QD
type: SiteQuality
SIO_000300: 1.008e1

VQSLOD
type: SiteQuality
SIO_000300: -2.231e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

GenotypeQuality
all individuals: 243
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 21266
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5594
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6922
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14478
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 742
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9012
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.611412062116287e-5
allele num: 55380
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.106954e6

VQSLOD
type: SiteQuality
SIO_000300: 7.61e-1

FS
type: SiteQuality
SIO_000300: 6.32e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.11e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.76e-1

QD
type: SiteQuality
SIO_000300: 1.353e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.2e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7760
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.559575795383656e-4
allele num: 6412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14002
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 726
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52054
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5334
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.11e-1

FS
type: SiteQuality
SIO_000300: 3.222e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.298e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.88e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.86e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.18e0

DP
type: SiteQuality
SIO_000300: 9.44625e5

GenotypeQuality
all individuals: 3564
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4557
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 482
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variant carriers: 6

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
all individuals: 3808
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
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variant carriers: 0

GenotypeQuality
all individuals: 1829
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.405916094927455e-4
allele num: 35564
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3876
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10974
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 534
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3904
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6270
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4000
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.34e0

QD
type: SiteQuality
SIO_000300: 1.106e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.74e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.78e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.71e-1

DP
type: SiteQuality
SIO_000300: 7.01834e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.381e0

VQSLOD
type: SiteQuality
SIO_000300: 6.76e-1

GenotypeQuality
all individuals: 112
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 163
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1016
bin: 2.5e0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3462
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 485
bin: 9.75e1
variant carriers: 9

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3682
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33960
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 524
num of homozygotes: 0

African
type: Population
allele count: 9
allele frequency: 1.511081262592344e-3
allele num: 5956
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3610
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10638
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.81e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

FS
type: SiteQuality
SIO_000300: 1.319e0

MQ
type: SiteQuality
SIO_000300: 5.911e1

MQRankSum
type: SiteQuality
SIO_000300: -5.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 6.90387e5

QD
type: SiteQuality
SIO_000300: 1.17e1

VQSLOD
type: SiteQuality
SIO_000300: 5.32e-1

GenotypeQuality
all individuals: 476
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14690
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 71
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variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2934
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3202
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.030869212022746e-4
allele num: 9848
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 30488
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.229e1

DP
type: SiteQuality
SIO_000300: 6.72591e5

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.06e-2

MQRankSum
type: SiteQuality
SIO_000300: 8.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.63e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 265
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 739
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2484
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3162
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8998
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2724
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.648037355902524e-5
allele num: 27412
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 446
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.39e0

DP
type: SiteQuality
SIO_000300: 6.58822e5

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.36e-2

QD
type: SiteQuality
SIO_000300: 1.787e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6436
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.84016973125884e-5
allele num: 11312
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66236
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.072614e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.165e0

VQSLOD
type: SiteQuality
SIO_000300: 8.110000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.38e-1

FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.286e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.268e0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 3957
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variant carriers: 0

GenotypeQuality
all individuals: 784
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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: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14371
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variant carriers: 1

GenotypeQuality
all individuals: 2189
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509753004408479e-5
allele num: 66236
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11312
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 8.110000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.165e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

QD
type: SiteQuality
SIO_000300: 1.286e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.268e0

DP
type: SiteQuality
SIO_000300: 2.072614e6

FS
type: SiteQuality
SIO_000300: 5.705e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1175
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2502
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2463
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2166
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14356
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 1737
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 776
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3283
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6507
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1635
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1224
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.118568232662192e-3
allele num: 894
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6426
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.020235578375113e-5
allele num: 66220
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11306
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.355e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.7e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.66e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

FS
type: SiteQuality
SIO_000300: 3.516e0

MQRankSum
type: SiteQuality
SIO_000300: -1.96e-1

DP
type: SiteQuality
SIO_000300: 2.0746e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.76e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.58e-1

GenotypeQuality
all individuals: 1169
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 781
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variant carriers: 0

GenotypeQuality
all individuals: 3263
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1726
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
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variant carriers: 0

GenotypeQuality
all individuals: 2439
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variant carriers: 0

GenotypeQuality
all individuals: 107
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variant carriers: 0

GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 14378
bin: 9.75e1
variant carriers: 28

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6487
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 599
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 29
allele frequency: 4.374321226016653e-4
allele num: 66296
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11328
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16280
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.4e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

DP
type: SiteQuality
SIO_000300: 2.077751e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

FS
type: SiteQuality
SIO_000300: 7.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.6e0

MQRankSum
type: SiteQuality
SIO_000300: 1.75e-1

QD
type: SiteQuality
SIO_000300: 1.479e1

MQ
type: SiteQuality
SIO_000300: 5.955e1

GenotypeQuality
all individuals: 47
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3315
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 886
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1663
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4029
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variant carriers: 0

GenotypeQuality
all individuals: 14387
bin: 9.75e1
variant carriers: 20

GenotypeQuality
all individuals: 1535
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2218
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17823
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 5.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.761804087385483e-4
allele num: 11352
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 19
allele frequency: 1.839303000968054e-3
allele num: 10330
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66354
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

DP
type: SiteQuality
SIO_000300: 2.094088e6

QD
type: SiteQuality
SIO_000300: 1.594e1

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.92e-1

GenotypeQuality
all individuals: 766
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1468
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3315
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 753
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17823
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2218
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1092
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1535
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3144
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14387
bin: 9.75e1
variant carriers: 7

African
type: Population
allele count: 1
allele frequency: 9.680542110358181e-5
allele num: 10330
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.028272598486903e-5
allele num: 66354
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.227144434899988e-4
allele num: 16298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.92e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.9e-2

FS
type: SiteQuality
SIO_000300: 7.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

QD
type: SiteQuality
SIO_000300: 1.594e1

DP
type: SiteQuality
SIO_000300: 2.094088e6

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

GenotypeQuality
all individuals: 19105
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6648
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 920
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 315
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variant carriers: 0

GenotypeQuality
all individuals: 4095
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variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
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variant carriers: 0

GenotypeQuality
all individuals: 457
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variant carriers: 0

GenotypeQuality
all individuals: 999
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3383
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10328
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16298
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507204437209863e-5
allele num: 66348
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.25e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.879999999999999e-1

FS
type: SiteQuality
SIO_000300: 2.183e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.23e0

QD
type: SiteQuality
SIO_000300: 1.236e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

DP
type: SiteQuality
SIO_000300: 2.10697e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 4492
bin: 6.75e1
variant carriers: 202

GenotypeQuality
all individuals: 13752
bin: 6.25e1
variant carriers: 226

GenotypeQuality
all individuals: 474
bin: 5.25e1
variant carriers: 182

GenotypeQuality
all individuals: 1980
bin: 8.25e1
variant carriers: 199

GenotypeQuality
all individuals: 110
bin: 2.5e0
variant carriers: 37

GenotypeQuality
all individuals: 420
bin: 4.25e1
variant carriers: 110

GenotypeQuality
all individuals: 60
bin: 7.5e0
variant carriers: 42

GenotypeQuality
all individuals: 1053
bin: 8.75e1
variant carriers: 135

GenotypeQuality
all individuals: 2042
bin: 7.25e1
variant carriers: 130

GenotypeQuality
all individuals: 2431
bin: 7.75e1
variant carriers: 223

GenotypeQuality
all individuals: 386
bin: 5.75e1
variant carriers: 133

GenotypeQuality
all individuals: 29495
bin: 9.75e1
variant carriers: 21927

Latino
type: Population
allele count: 2873
allele frequency: 2.537089367714588e-1
allele num: 11324
num of homozygotes: 348

European (Finnish)
type: Population
allele count: 1441
allele frequency: 2.229959764778706e-1
allele num: 6462
num of homozygotes: 154

African
type: Population
allele count: 3199
allele frequency: 3.093810444874275e-1
allele num: 10340
num of homozygotes: 511

Other
type: Population
allele count: 210
allele frequency: 2.34375e-1
allele num: 896
num of homozygotes: 31

European (Non-Finnish)
type: Population
allele count: 14048
allele frequency: 2.119173329310605e-1
allele num: 66290
num of homozygotes: 1431

South Asian
type: Population
allele count: 4206
allele frequency: 2.568392769907181e-1
allele num: 16376
num of homozygotes: 564

East Asian
type: Population
allele count: 1236
allele frequency: 1.435206688341849e-1
allele num: 8612
num of homozygotes: 91

FS
type: SiteQuality
SIO_000300: 2.448e0

DP
type: SiteQuality
SIO_000300: 2.329149e6

QD
type: SiteQuality
SIO_000300: 1.411e1

VQSLOD
type: SiteQuality
SIO_000300: 2.97e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.44e-2

MQ
type: SiteQuality
SIO_000300: 5.953e1

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4015
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 444
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1768
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16230
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 499
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2655
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18224
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66536
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11464
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.63948332369385e-5
allele num: 10374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.98e0

DP
type: SiteQuality
SIO_000300: 2.312877e6

FS
type: SiteQuality
SIO_000300: 2.171e0

MQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.129e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.938e1

QD
type: SiteQuality
SIO_000300: 1.826e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.49e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.44e-1

GenotypeQuality
all individuals: 9
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6184
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 2934
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variant carriers: 0

GenotypeQuality
all individuals: 3440
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 293
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2662
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 532
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variant carriers: 0

GenotypeQuality
all individuals: 882
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16404
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.641342074816814e-5
allele num: 10372
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66532
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.155e0

QD
type: SiteQuality
SIO_000300: 2.208e1

VQSLOD
type: SiteQuality
SIO_000300: 1.81e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.17e-1

DP
type: SiteQuality
SIO_000300: 2.316856e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.135e0

GenotypeQuality
all individuals: 4049
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 186
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 712
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18256
bin: 9.75e1
variant carriers: 29

GenotypeQuality
all individuals: 6223
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 466
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1783
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2958
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 27
allele frequency: 3.127171646977068e-3
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10378
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6522
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66554
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.092360180333861e-5
allele num: 16414
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.31e-1

MQ
type: SiteQuality
SIO_000300: 5.962e1

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.95e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.29e-1

QD
type: SiteQuality
SIO_000300: 1.159e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.494e0

DP
type: SiteQuality
SIO_000300: 2.322049e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.37e-1

GenotypeQuality
all individuals: 19
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17635
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2954
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1788
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6223
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4058
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3458
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18239
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004717406327935e-5
allele num: 66562
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11488
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -4.01e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.918e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.49e-1

FS
type: SiteQuality
SIO_000300: 2.611e0

QD
type: SiteQuality
SIO_000300: 8.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.76e-1

DP
type: SiteQuality
SIO_000300: 2.325645e6

VQSLOD
type: SiteQuality
SIO_000300: -1.38e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4694
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1064
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2499
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1445
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 253
bin: 3.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.355299219950005e-4
allele num: 66406
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.4330900243309e-4
allele num: 16440
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.541266e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.19e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.58e-1

FS
type: SiteQuality
SIO_000300: 2.072e0

QD
type: SiteQuality
SIO_000300: 1.486e1

GenotypeQuality
all individuals: 1064
bin: 8.75e1
variant carriers: 104

GenotypeQuality
all individuals: 2140
bin: 7.25e1
variant carriers: 87

GenotypeQuality
all individuals: 29553
bin: 9.75e1
variant carriers: 21618

GenotypeQuality
all individuals: 169
bin: 2.75e1
variant carriers: 25

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 27

GenotypeQuality
all individuals: 196
bin: 4.25e1
variant carriers: 67

GenotypeQuality
all individuals: 15063
bin: 6.25e1
variant carriers: 121

GenotypeQuality
all individuals: 4694
bin: 6.75e1
variant carriers: 166

GenotypeQuality
all individuals: 2026
bin: 8.25e1
variant carriers: 141

GenotypeQuality
all individuals: 1445
bin: 9.25e1
variant carriers: 151

GenotypeQuality
all individuals: 331
bin: 3.75e1
variant carriers: 82

GenotypeQuality
all individuals: 61
bin: 1.75e1
variant carriers: 35

Other
type: Population
allele count: 206
allele frequency: 2.283813747228381e-1
allele num: 902
num of homozygotes: 29

East Asian
type: Population
allele count: 1201
allele frequency: 1.392948271862677e-1
allele num: 8622
num of homozygotes: 83

European (Non-Finnish)
type: Population
allele count: 14135
allele frequency: 2.12857271933259e-1
allele num: 66406
num of homozygotes: 1459

African
type: Population
allele count: 1798
allele frequency: 1.733847637415622e-1
allele num: 10370
num of homozygotes: 159

Latino
type: Population
allele count: 2811
allele frequency: 2.45974798739937e-1
allele num: 11428
num of homozygotes: 332

European (Finnish)
type: Population
allele count: 1449
allele frequency: 2.227859778597786e-1
allele num: 6504
num of homozygotes: 155

South Asian
type: Population
allele count: 4246
allele frequency: 2.582725060827251e-1
allele num: 16440
num of homozygotes: 575

VQSLOD
type: SiteQuality
SIO_000300: 3.19e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.58e-1

FS
type: SiteQuality
SIO_000300: 2.072e0

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

DP
type: SiteQuality
SIO_000300: 2.541266e6

MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.12e-2

QD
type: SiteQuality
SIO_000300: 1.486e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.7e-2

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21131
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1642
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 294
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3121
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7161
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16265
bin: 9.75e1
variant carriers: 139

GenotypeQuality
all individuals: 284
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 10
allele frequency: 8.674531575294934e-4
allele num: 11528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

African
type: Population
allele count: 130
allele frequency: 1.251443973815941e-2
allele num: 10388
num of homozygotes: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16452
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6552
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

MQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

DP
type: SiteQuality
SIO_000300: 2.215414e6

BaseQRankSum
type: SiteQuality
SIO_000300: 7.0e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.19e-1

FS
type: SiteQuality
SIO_000300: 2.797e0

QD
type: SiteQuality
SIO_000300: 1.317e1

GenotypeQuality
all individuals: 178
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16176
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 3195
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3124
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2273
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 315
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3938
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1646
bin: 8.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.215953307392996e-4
allele num: 16448
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.813246053138236e-4
allele num: 10388
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: 11532
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50105073551486e-5
allele num: 66620
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.22e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.29e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.41e-1

QD
type: SiteQuality
SIO_000300: 1.284e1

DP
type: SiteQuality
SIO_000300: 2.213715e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQ
type: SiteQuality
SIO_000300: 5.92e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.82e0

GenotypeQuality
all individuals: 142
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16180
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2265
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 133
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3930
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3221
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21720
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11532
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16468
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -4.59e-1

DP
type: SiteQuality
SIO_000300: 2.217231e6

MQ
type: SiteQuality
SIO_000300: 5.893e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.13e-1

QD
type: SiteQuality
SIO_000300: 1.009e1

MQRankSum
type: SiteQuality
SIO_000300: 2.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 1.575e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.362e0

GenotypeQuality
all individuals: 107
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16181
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2265
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 184
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 136
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3919
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 230
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7245
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1650
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 139
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3132
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66658
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16472
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

VQSLOD
type: SiteQuality
SIO_000300: 9.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.76e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

DP
type: SiteQuality
SIO_000300: 2.218632e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 3.458e0

MQRankSum
type: SiteQuality
SIO_000300: -3.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.64e0

QD
type: SiteQuality
SIO_000300: 1.249e1

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

GenotypeQuality
all individuals: 124
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 105
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7251
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21940
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 16182
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1654
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3910
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3129
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2266
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
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: 11536
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.49e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

MQ
type: SiteQuality
SIO_000300: 5.881e1

DP
type: SiteQuality
SIO_000300: 2.222117e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.745e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -5.122e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.13e-1

GenotypeQuality
all individuals: 3128
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3904
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3232
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16183
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 92
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 172
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1653
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2267
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
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: 6594
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.49985000299994e-5
allele num: 66668
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.01e-1

DP
type: SiteQuality
SIO_000300: 2.222583e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

FS
type: SiteQuality
SIO_000300: 4.632e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.229e0

QD
type: SiteQuality
SIO_000300: 1.171e1

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 3.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499235130027895e-5
allele num: 66678
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.81e-1

FS
type: SiteQuality
SIO_000300: 1.184e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.53e-1

QD
type: SiteQuality
SIO_000300: 1.515e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

VQSLOD
type: SiteQuality
SIO_000300: 9.9e-2

DP
type: SiteQuality
SIO_000300: 2.223919e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3128
bin: 8.25e1
variant carriers: 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: 906
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.069434328720563e-5
allele num: 16476
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -8.120000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.213e0

QD
type: SiteQuality
SIO_000300: 1.096e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.438e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.570000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 3.02e-1

DP
type: SiteQuality
SIO_000300: 2.225322e6

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 189
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variant carriers: 0

GenotypeQuality
all individuals: 3177
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 58
allele frequency: 5.023384721981639e-3
allele num: 11546
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.738e0

DP
type: SiteQuality
SIO_000300: 2.225903e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.08e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.13e-1

QD
type: SiteQuality
SIO_000300: 1.455e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.03e-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

GenotypeQuality
all individuals: 3163
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GenotypeQuality
all individuals: 195
bin: 2.25e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16474
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.118e1

FS
type: SiteQuality
SIO_000300: 1.013e0

VQSLOD
type: SiteQuality
SIO_000300: 5.580000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e0

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQ
type: SiteQuality
SIO_000300: 5.915e1

DP
type: SiteQuality
SIO_000300: 2.224793e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.38e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 21891
bin: 6.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.070171178827243e-5
allele num: 16474
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.053268765133172e-4
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999580058791769e-5
allele num: 66676
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.24e0

VQSLOD
type: SiteQuality
SIO_000300: 5.37e0

QD
type: SiteQuality
SIO_000300: 1.414e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.225064e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 28

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 18
allele frequency: 1.092630812188904e-3
allele num: 16474
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.053268765133172e-4
allele num: 6608
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.000240009600384e-5
allele num: 66664
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.11e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.15e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.68e0

DP
type: SiteQuality
SIO_000300: 2.226051e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.52e-1

FS
type: SiteQuality
SIO_000300: 1.745e0

QD
type: SiteQuality
SIO_000300: 1.284e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 4
allele frequency: 2.427773731488225e-4
allele num: 16476
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999220202747286e-5
allele num: 66684
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.225337e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.56e-2

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.0095e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.564e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

QD
type: SiteQuality
SIO_000300: 2.058e1

MQ
type: SiteQuality
SIO_000300: 5.933e1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16476
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8650
num of homozygotes: 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: 11550
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499640028797696e-5
allele num: 66672
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.144e0

DP
type: SiteQuality
SIO_000300: 2.225575e6

FS
type: SiteQuality
SIO_000300: 1.032e0

VQSLOD
type: SiteQuality
SIO_000300: 7.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.14e-1

QD
type: SiteQuality
SIO_000300: 1.198e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.75e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
all individuals: 3110
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GenotypeQuality
all individuals: 3800
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 214
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3123
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 10
allele frequency: 6.069434328720563e-4
allele num: 16476
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499370088187654e-5
allele num: 66676
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
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: 5.977e1

VQSLOD
type: SiteQuality
SIO_000300: 4.84e0

QD
type: SiteQuality
SIO_000300: 1.336e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.99e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.03e-1

DP
type: SiteQuality
SIO_000300: 2.226137e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.58e-1

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

GenotypeQuality
all individuals: 130
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
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2253
bin: 9.25e1
variant carriers: 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: 906
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499655079331754e-5
allele num: 66682
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.225644e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 2.5878e1

MQRankSum
type: SiteQuality
SIO_000300: 6.79e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -3.398e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.267e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.03e-1

QD
type: SiteQuality
SIO_000300: 1.466e1

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

GenotypeQuality
all individuals: 3
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3129
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7143
bin: 6.75e1
variant carriers: 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: 11554
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16482
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -7.606000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.277e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

MQRankSum
type: SiteQuality
SIO_000300: -1.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.034e0

FS
type: SiteQuality
SIO_000300: 2.726e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.15e-2

QD
type: SiteQuality
SIO_000300: 1.938e1

DP
type: SiteQuality
SIO_000300: 2.226026e6

GenotypeQuality
all individuals: 1650
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 121
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variant carriers: 0

GenotypeQuality
all individuals: 16169
bin: 9.75e1
variant carriers: 1

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.73e-1

MQ
type: SiteQuality
SIO_000300: 5.873e1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.500000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 8.706e0

DP
type: SiteQuality
SIO_000300: 2.226536e6

QD
type: SiteQuality
SIO_000300: 3.01e0

MQRankSum
type: SiteQuality
SIO_000300: 1.79e0

VQSLOD
type: SiteQuality
SIO_000300: -2.221e0

GenotypeQuality
all individuals: 101
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3796
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variant carriers: 0

GenotypeQuality
all individuals: 97
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variant carriers: 0

GenotypeQuality
all individuals: 3
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GenotypeQuality
all individuals: 75
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 121
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2252
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variant carriers: 0

GenotypeQuality
all individuals: 22544
bin: 6.25e1
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GenotypeQuality
all individuals: 118
bin: 3.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.213297743266198e-4
allele num: 16484
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
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: 8650
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 6.1e-2

DP
type: SiteQuality
SIO_000300: 2.226514e6

QD
type: SiteQuality
SIO_000300: 1.368e1

FS
type: SiteQuality
SIO_000300: 8.119e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.953e1

MQRankSum
type: SiteQuality
SIO_000300: -3.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.679999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.194e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-1

GenotypeQuality
all individuals: 124
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 91
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 138
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GenotypeQuality
all individuals: 22726
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 16168
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variant carriers: 1

GenotypeQuality
all individuals: 108
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GenotypeQuality
all individuals: 66
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variant carriers: 0

GenotypeQuality
all individuals: 3092
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variant carriers: 0

GenotypeQuality
all individuals: 3094
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.8e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

DP
type: SiteQuality
SIO_000300: 2.227044e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.44e-1

QD
type: SiteQuality
SIO_000300: 1.173e1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 82
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 100

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7068
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GenotypeQuality
all individuals: 95
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 5
allele frequency: 4.807692307692308e-4
allele num: 10400
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.652015919709292e-5
allele num: 11558
num of homozygotes: 0

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

South Asian
type: Population
allele count: 90
allele frequency: 5.459177483925755e-3
allele num: 16486
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.999520038396928e-5
allele num: 66672
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.7e-2

QD
type: SiteQuality
SIO_000300: 1.356e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.91e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

DP
type: SiteQuality
SIO_000300: 2.228058e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.1e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7074
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GenotypeQuality
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GenotypeQuality
all individuals: 16168
bin: 9.75e1
variant carriers: 4

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499745043342632e-5
allele num: 66678
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 3
allele frequency: 1.819725827975252e-4
allele num: 16486
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.861e0

QD
type: SiteQuality
SIO_000300: 1.28e1

MQRankSum
type: SiteQuality
SIO_000300: 4.4e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.59e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 3.72e-1

DP
type: SiteQuality
SIO_000300: 2.225448e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 101
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GenotypeQuality
all individuals: 3090
bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66678
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

MQ
type: SiteQuality
SIO_000300: 5.787e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.824e0

VQSLOD
type: SiteQuality
SIO_000300: -2.325e0

FS
type: SiteQuality
SIO_000300: 4.631e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.15e0

QD
type: SiteQuality
SIO_000300: 1.434e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.761e0

DP
type: SiteQuality
SIO_000300: 2.225308e6

GenotypeQuality
all individuals: 46
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 62
bin: 2.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1649
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3782
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23002
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3070
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2250
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3095
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16165
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16486
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.225272e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.89e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.56e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.0e-2

QD
type: SiteQuality
SIO_000300: 1.725e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.91e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

GenotypeQuality
all individuals: 3044
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6993
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3740
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22814
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 132
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2254
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16165
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3083
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.504639778972342e-5
allele num: 66598
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16470
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

DP
type: SiteQuality
SIO_000300: 2.223043e6

QD
type: SiteQuality
SIO_000300: 1.124e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.075e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.49e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.8e-2

FS
type: SiteQuality
SIO_000300: 2.43e0

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

GenotypeQuality
all individuals: 90
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 4.75e1
variant carriers: 0

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

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

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

GenotypeQuality
all individuals: 2254
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6985
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16170
bin: 9.75e1
variant carriers: 4

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

GenotypeQuality
all individuals: 22782
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3044
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 2.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501501501501501e-5
allele num: 66600
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10366
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21447656060238e-4
allele num: 16468
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.5e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.941e1

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.07e-1

DP
type: SiteQuality
SIO_000300: 2.222588e6

VQSLOD
type: SiteQuality
SIO_000300: 2.55e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.093e1

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

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1648
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2251
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 97
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16178
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 152
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6965
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3732
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22803
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 3.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66580
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

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

Latino
type: Population
allele count: 14
allele frequency: 1.21317157712305e-3
allele num: 11540
num of homozygotes: 1

South Asian
type: Population
allele count: 1
allele frequency: 6.073858114674441e-5
allele num: 16464
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.73e-2

DP
type: SiteQuality
SIO_000300: 2.221632e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.94e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: 2.79e0

MQRankSum
type: SiteQuality
SIO_000300: 5.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.15e-1

QD
type: SiteQuality
SIO_000300: 1.261e1

GenotypeQuality
all individuals: 88
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 166
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3037
bin: 7.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2242
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6951
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3720
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22689
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.25e1
variant carriers: 0

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

African
type: Population
allele count: 4
allele frequency: 3.863987635239567e-4
allele num: 10352
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.024803387779795e-4
allele num: 6612
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.334257975034674e-4
allele num: 11536
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.470615455807496e-4
allele num: 8644
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.073858114674441e-5
allele num: 16464
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 129
allele frequency: 1.937926268665685e-3
allele num: 66566
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.224931e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.33e-2

MQ
type: SiteQuality
SIO_000300: 5.967e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.24e-1

QD
type: SiteQuality
SIO_000300: 1.239e1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.6e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.71e-1

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

GenotypeQuality
all individuals: 2
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 54
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3726
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1643
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6955
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variant carriers: 0

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

GenotypeQuality
all individuals: 139
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3036
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22780
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16157
bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 336
bin: 2.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.35196034249662e-4
allele num: 66570
num of homozygotes: 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: 16462
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
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: 10352
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

DP
type: SiteQuality
SIO_000300: 2.221323e6

FS
type: SiteQuality
SIO_000300: 1.745e0

QD
type: SiteQuality
SIO_000300: 1.13e1

MQ
type: SiteQuality
SIO_000300: 5.954e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

MQRankSum
type: SiteQuality
SIO_000300: 7.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.69e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.66e-1

GenotypeQuality
all individuals: 7
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 16160
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 121
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6904
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 380
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22472
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3076
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16454
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 9.667440061871617e-5
allele num: 10344
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 7
allele frequency: 1.052030418708107e-4
allele num: 66538
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.27e-1

DP
type: SiteQuality
SIO_000300: 2.219772e6

FS
type: SiteQuality
SIO_000300: 3.304e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.135e1

MQ
type: SiteQuality
SIO_000300: 5.954e1

MQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.55e0

GenotypeQuality
all individuals: 427
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22684
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16154
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3020
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 131
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variant carriers: 0

GenotypeQuality
all individuals: 6890
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variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3076
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variant carriers: 0

GenotypeQuality
all individuals: 2240
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3704
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66500
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.31535077564251e-4
allele num: 8638
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.79e-1

DP
type: SiteQuality
SIO_000300: 2.218394e6

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

QD
type: SiteQuality
SIO_000300: 1.217e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.34e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

FS
type: SiteQuality
SIO_000300: 2.451e0

VQSLOD
type: SiteQuality
SIO_000300: 2.61e0

GenotypeQuality
all individuals: 427
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3076
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16154
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2240
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1640
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3704
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6890
bin: 6.75e1
variant carriers: 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: 6612
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503759398496241e-5
allele num: 66500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.947e1

QD
type: SiteQuality
SIO_000300: 1.217e1

FS
type: SiteQuality
SIO_000300: 2.451e0

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.61e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.34e-1

DP
type: SiteQuality
SIO_000300: 2.218394e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.79e-1

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3076
bin: 8.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007518796992481e-5
allele num: 66500
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 2.451e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

MQRankSum
type: SiteQuality
SIO_000300: 2.01e-1

DP
type: SiteQuality
SIO_000300: 2.218394e6

VQSLOD
type: SiteQuality
SIO_000300: 2.61e0

QD
type: SiteQuality
SIO_000300: 1.217e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.673026886383348e-5
allele num: 11530
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66494
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.06e-1

FS
type: SiteQuality
SIO_000300: 8.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.68e-1

QD
type: SiteQuality
SIO_000300: 1.162e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 9.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.291e0

DP
type: SiteQuality
SIO_000300: 2.217266e6

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3074
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.023913370431643e-5
allele num: 66490
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.009e1

VQSLOD
type: SiteQuality
SIO_000300: 1.06e0

DP
type: SiteQuality
SIO_000300: 2.216937e6

MQ
type: SiteQuality
SIO_000300: 5.913e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.48e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 2.552e0

MQRankSum
type: SiteQuality
SIO_000300: -3.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.66e-1

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

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

GenotypeQuality
all individuals: 3002
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 252
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3059
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variant carriers: 0

GenotypeQuality
all individuals: 16157
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 1638
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16448
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.84027105517909e-4
allele num: 10330
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.683570684265369e-5
allele num: 11516
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66450
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.083e1

VQSLOD
type: SiteQuality
SIO_000300: 4.33e0

MQRankSum
type: SiteQuality
SIO_000300: 4.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.08e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

DP
type: SiteQuality
SIO_000300: 2.214028e6

GenotypeQuality
all individuals: 22610
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16155
bin: 9.75e1
variant carriers: 4

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 10
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GenotypeQuality
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GenotypeQuality
all individuals: 3683
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variant carriers: 0

GenotypeQuality
all individuals: 2994
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 3
allele frequency: 2.904162633107454e-4
allele num: 10330
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: 6.079766536964981e-5
allele num: 16448
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66448
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 2.313e1

DP
type: SiteQuality
SIO_000300: 2.214059e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.74e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.5e-2

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.77e-1

GenotypeQuality
all individuals: 612
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
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GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6793
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GenotypeQuality
all individuals: 184
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 16152
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 3057
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
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: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505434618974498e-5
allele num: 66426
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: 10324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16444
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.075e0

VQSLOD
type: SiteQuality
SIO_000300: 3.95e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e0

QD
type: SiteQuality
SIO_000300: 1.121e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.19e-1

DP
type: SiteQuality
SIO_000300: 2.211087e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.76e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.69e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6775
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16157
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2235
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
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: 11512
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66412
num of homozygotes: 0

South Asian
type: Population
allele count: 14
allele frequency: 8.513743614692289e-4
allele num: 16444
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.97e1

QD
type: SiteQuality
SIO_000300: 1.438e1

FS
type: SiteQuality
SIO_000300: 5.4e-1

DP
type: SiteQuality
SIO_000300: 2.210878e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.39e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

GenotypeQuality
all individuals: 22166
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2234
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 243
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3664
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3057
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
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: 1.507113576079093e-5
allele num: 66352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.206288e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.044e0

MQRankSum
type: SiteQuality
SIO_000300: 4.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.06e-1

QD
type: SiteQuality
SIO_000300: 1.107e1

FS
type: SiteQuality
SIO_000300: 3.447e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.63e-1

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22041
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2233
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 274
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 805
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3052
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1641
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2961
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
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: 10308
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16422
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.692628650904033e-5
allele num: 11504
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.94e0

QD
type: SiteQuality
SIO_000300: 1.061e1

VQSLOD
type: SiteQuality
SIO_000300: -2.046e0

FS
type: SiteQuality
SIO_000300: 1.2621e1

DP
type: SiteQuality
SIO_000300: 2.204044e6

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.652e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.81e-1

GenotypeQuality
all individuals: 3632
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16153
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6615
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3045
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1639
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2234
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21439
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508295625942685e-5
allele num: 66300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16416
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: 10300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 9.890000000000001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

MQ
type: SiteQuality
SIO_000300: 5.989e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.78e-1

DP
type: SiteQuality
SIO_000300: 2.197606e6

VQSLOD
type: SiteQuality
SIO_000300: 6.3e-1

FS
type: SiteQuality
SIO_000300: 2.67e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.673e0