11-86382864-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382864
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382864
    reference: chr 11
allele count: 1
allele frequency: 8.474719910506958e-6
allele num: 117998
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000534638
  gene symbol: ME3
  hgvsc: ENST00000534638.1:n.1G>A
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.144G>A
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.123G>A
  hgvsp: ENST00000543262.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.123G>A
  hgvsp: ENST00000526504.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.123G>A
  hgvsp: ENST00000526944.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.123G>A
  hgvsp: ENST00000524826.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.123G>A
  hgvsp: ENST00000530335.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.123G>A
  hgvsp: ENST00000526834.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.123G>A
  hgvsp: ENST00000532471.1:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.123G>A
  hgvsp: ENST00000393324.3:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.123G>A
  hgvsp: ENST00000359636.2:c.123G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4090
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1371
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38186
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14410
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala41Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum

11-86382874-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382874
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382874
    reference: chr 11
allele count: 4
allele frequency: 3.419504855696895e-5
allele num: 116976
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.113C>T
  hgvsp: ENSP00000440246.1:p.Pro38Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.113C>T
  hgvsp: ENSP00000437204.1:p.Pro38Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.113C>T
  hgvsp: ENSP00000434690.1:p.Pro38Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.113C>T
  hgvsp: ENSP00000376998.2:p.Pro38Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.113C>T
  hgvsp: ENSP00000435427.1:p.Pro38Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.113C>T
  hgvsp: ENSP00000352657.2:p.Pro38Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.113C>T
  hgvsp: ENSP00000433636.1:p.Pro38Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.113C>T
  hgvsp: ENSP00000431182.1:p.Pro38Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.113C>T
  hgvsp: ENSP00000434431.1:p.Pro38Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.134C>T
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4056
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14021
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Pro38Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-86382896-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382896
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382896
    reference: chr 11
allele count: 1
allele frequency: 8.934953538241601e-6
allele num: 111920
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.91G>T
  hgvsp: ENSP00000434690.1:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.112G>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.91G>T
  hgvsp: ENSP00000440246.1:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.91G>T
  hgvsp: ENSP00000376998.2:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.91G>T
  hgvsp: ENSP00000435427.1:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.91G>T
  hgvsp: ENSP00000431182.1:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.91G>T
  hgvsp: ENSP00000352657.2:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.91G>T
  hgvsp: ENSP00000433636.1:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.91G>T
  hgvsp: ENSP00000437204.1:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.91G>T
  hgvsp: ENSP00000434431.1:p.Ala31Ser
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5964
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala31Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

11-86382896-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382896
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382896
    reference: chr 11
allele count: 1
allele frequency: 8.934953538241601e-6
allele num: 111920
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.91G>A
  hgvsp: ENSP00000433636.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.91G>A
  hgvsp: ENSP00000434690.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.91G>A
  hgvsp: ENSP00000431182.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.91G>A
  hgvsp: ENSP00000434431.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.91G>A
  hgvsp: ENSP00000352657.2:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.91G>A
  hgvsp: ENSP00000440246.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.91G>A
  hgvsp: ENSP00000437204.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.91G>A
  hgvsp: ENSP00000435427.1:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.112G>A
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.91G>A
  hgvsp: ENSP00000376998.2:p.Ala31Thr
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1382
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32196
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5964
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala31Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

11-86382897-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382897
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382897
    reference: chr 11
allele count: 2
allele frequency: 1.803751803751804e-5
allele num: 110880
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.111C>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.90C>T
  hgvsp: ENST00000526504.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.90C>T
  hgvsp: ENST00000532471.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.90C>T
  hgvsp: ENST00000359636.2:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.90C>T
  hgvsp: ENST00000530335.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.90C>T
  hgvsp: ENST00000543262.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.90C>T
  hgvsp: ENST00000524826.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.90C>T
  hgvsp: ENST00000393324.3:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.90C>T
  hgvsp: ENST00000526834.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.90C>T
  hgvsp: ENST00000526944.1:c.90C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 952
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro30Pro
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS

11-86382897-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382897
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382897
    reference: chr 11
allele count: 1
allele frequency: 9.018759018759019e-6
allele num: 110880
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.90C>G
  hgvsp: ENST00000526944.1:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.90C>G
  hgvsp: ENST00000530335.1:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.90C>G
  hgvsp: ENST00000526504.1:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.90C>G
  hgvsp: ENST00000393324.3:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.90C>G
  hgvsp: ENST00000543262.1:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.90C>G
  hgvsp: ENST00000526834.1:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.90C>G
  hgvsp: ENST00000524826.1:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.90C>G
  hgvsp: ENST00000532471.1:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.90C>G
  hgvsp: ENST00000359636.2:c.90C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.111C>G
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1523
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30490
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2979
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Pro30Pro
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

11-86382901-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382901
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382901
    reference: chr 11
allele count: 1
allele frequency: 9.108297659167501e-6
allele num: 109790
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.86C>A
  hgvsp: ENSP00000376998.2:p.Ala29Glu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.86C>A
  hgvsp: ENSP00000352657.2:p.Ala29Glu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.86C>A
  hgvsp: ENSP00000433636.1:p.Ala29Glu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.86C>A
  hgvsp: ENSP00000435427.1:p.Ala29Glu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.86C>A
  hgvsp: ENSP00000431182.1:p.Ala29Glu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.86C>A
  hgvsp: ENSP00000434690.1:p.Ala29Glu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.86C>A
  hgvsp: ENSP00000437204.1:p.Ala29Glu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.86C>A
  hgvsp: ENSP00000434431.1:p.Ala29Glu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.86C>A
  hgvsp: ENSP00000440246.1:p.Ala29Glu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.107C>A
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10830
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3761
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3214
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11667
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala29Glu
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP

11-86382904-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382904
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382904
    reference: chr 11
allele count: 1
allele frequency: 9.192866335723479e-6
allele num: 108780
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.83C>A
  hgvsp: ENSP00000435427.1:p.Thr28Asn
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.83C>A
  hgvsp: ENSP00000437204.1:p.Thr28Asn
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.83C>A
  hgvsp: ENSP00000434431.1:p.Thr28Asn
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.83C>A
  hgvsp: ENSP00000440246.1:p.Thr28Asn
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.83C>A
  hgvsp: ENSP00000431182.1:p.Thr28Asn
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.83C>A
  hgvsp: ENSP00000434690.1:p.Thr28Asn
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.83C>A
  hgvsp: ENSP00000376998.2:p.Thr28Asn
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.83C>A
  hgvsp: ENSP00000433636.1:p.Thr28Asn
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.104C>A
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.83C>A
  hgvsp: ENSP00000352657.2:p.Thr28Asn
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9982
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3062
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10211
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4650
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26363
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr28Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: QD

11-86382909-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382909
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382909
    reference: chr 11
allele count: 1
allele frequency: 9.628160443665633e-6
allele num: 103862
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.78A>G
  hgvsp: ENST00000526944.1:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.78A>G
  hgvsp: ENST00000543262.1:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.78A>G
  hgvsp: ENST00000524826.1:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.78A>G
  hgvsp: ENST00000393324.3:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.78A>G
  hgvsp: ENST00000532471.1:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.78A>G
  hgvsp: ENST00000526504.1:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.99A>G
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.78A>G
  hgvsp: ENST00000526834.1:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.78A>G
  hgvsp: ENST00000359636.2:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.78A>G
  hgvsp: ENST00000530335.1:c.78A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2421
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8280
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15986
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6972
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 718
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr26Thr
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff

11-86382915-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382915
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382915
    reference: chr 11
allele count: 1
allele frequency: 1.125163148656555e-5
allele num: 88876
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.72C>T
  hgvsp: ENST00000532471.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.72C>T
  hgvsp: ENST00000543262.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.72C>T
  hgvsp: ENST00000530335.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.72C>T
  hgvsp: ENST00000526944.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.72C>T
  hgvsp: ENST00000393324.3:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.72C>T
  hgvsp: ENST00000524826.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.72C>T
  hgvsp: ENST00000526504.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.93C>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.72C>T
  hgvsp: ENST00000526834.1:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.72C>T
  hgvsp: ENST00000359636.2:c.72C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3746
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1109
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg24Arg
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

11-86382915-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382915
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382915
    reference: chr 11
allele count: 1
allele frequency: 1.125163148656555e-5
allele num: 88876
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.72C>G
  hgvsp: ENST00000393324.3:c.72C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.72C>G
  hgvsp: ENST00000526504.1:c.72C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.72C>G
  hgvsp: ENST00000543262.1:c.72C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.72C>G
  hgvsp: ENST00000526834.1:c.72C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.72C>G
  hgvsp: ENST00000359636.2:c.72C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.72C>G
  hgvsp: ENST00000524826.1:c.72C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.72C>G
  hgvsp: ENST00000530335.1:c.72C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.72C>G
  hgvsp: ENST00000532471.1:c.72C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.72C>G
  hgvsp: ENST00000526944.1:c.72C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.93C>G
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3746
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8355
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3467
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19940
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg24Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP

http://identifiers.org/exac.variant/11-86382916-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382916
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382916
    reference: chr 11
allele count: 2
allele frequency: 2.261727054779029e-5
allele num: 88428
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.71G>T
  hgvsp: ENSP00000434690.1:p.Arg24Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.71G>T
  hgvsp: ENSP00000376998.2:p.Arg24Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.71G>T
  hgvsp: ENSP00000434431.1:p.Arg24Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.92G>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.71G>T
  hgvsp: ENSP00000433636.1:p.Arg24Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.71G>T
  hgvsp: ENSP00000352657.2:p.Arg24Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.71G>T
  hgvsp: ENSP00000431182.1:p.Arg24Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.71G>T
  hgvsp: ENSP00000435427.1:p.Arg24Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.71G>T
  hgvsp: ENSP00000437204.1:p.Arg24Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.71G>T
  hgvsp: ENSP00000440246.1:p.Arg24Leu
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8936
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12376
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19992
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg24Leu
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

11-86382916-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382916
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382916
    reference: chr 11
allele count: 2
allele frequency: 2.261727054779029e-5
allele num: 88428
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.71G>A
  hgvsp: ENSP00000433636.1:p.Arg24His
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.71G>A
  hgvsp: ENSP00000431182.1:p.Arg24His
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.71G>A
  hgvsp: ENSP00000435427.1:p.Arg24His
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.71G>A
  hgvsp: ENSP00000376998.2:p.Arg24His
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.71G>A
  hgvsp: ENSP00000440246.1:p.Arg24His
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.71G>A
  hgvsp: ENSP00000437204.1:p.Arg24His
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.71G>A
  hgvsp: ENSP00000434690.1:p.Arg24His
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.92G>A
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.71G>A
  hgvsp: ENSP00000434431.1:p.Arg24His
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.71G>A
  hgvsp: ENSP00000352657.2:p.Arg24His
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19992
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8936
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg24His
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

11-86382919-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382919
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382919
    reference: chr 11
allele count: 3
allele frequency: 3.385240352064997e-5
allele num: 88620
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.68C>T
  hgvsp: ENSP00000434690.1:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.68C>T
  hgvsp: ENSP00000433636.1:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.68C>T
  hgvsp: ENSP00000435427.1:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.68C>T
  hgvsp: ENSP00000376998.2:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.68C>T
  hgvsp: ENSP00000431182.1:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.68C>T
  hgvsp: ENSP00000434431.1:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.68C>T
  hgvsp: ENSP00000437204.1:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.89C>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.68C>T
  hgvsp: ENSP00000440246.1:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.68C>T
  hgvsp: ENSP00000352657.2:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3578
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11991
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20243
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8658
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8650
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro23Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-86382926-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382926
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382926
    reference: chr 11
allele count: 1
allele frequency: 1.595252528475258e-5
allele num: 62686
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.61G>T
  hgvsp: ENSP00000435427.1:p.Ala21Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.61G>T
  hgvsp: ENSP00000434431.1:p.Ala21Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.61G>T
  hgvsp: ENSP00000440246.1:p.Ala21Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.61G>T
  hgvsp: ENSP00000431182.1:p.Ala21Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.61G>T
  hgvsp: ENSP00000437204.1:p.Ala21Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.61G>T
  hgvsp: ENSP00000433636.1:p.Ala21Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.61G>T
  hgvsp: ENSP00000434690.1:p.Ala21Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.82G>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.61G>T
  hgvsp: ENSP00000376998.2:p.Ala21Ser
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.61G>T
  hgvsp: ENSP00000352657.2:p.Ala21Ser
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13867
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9833
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala21Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum

11-86382926-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382926
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382926
    reference: chr 11
allele count: 5
allele frequency: 7.976262642376288e-5
allele num: 62686
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.61G>A
  hgvsp: ENSP00000435427.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.61G>A
  hgvsp: ENSP00000437204.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.61G>A
  hgvsp: ENSP00000434431.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.61G>A
  hgvsp: ENSP00000376998.2:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.61G>A
  hgvsp: ENSP00000434690.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.61G>A
  hgvsp: ENSP00000431182.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.82G>A
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.61G>A
  hgvsp: ENSP00000352657.2:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.61G>A
  hgvsp: ENSP00000433636.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.61G>A
  hgvsp: ENSP00000440246.1:p.Ala21Thr
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5314
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19200
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1574
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13867
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9833
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1776
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala21Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

11-86382927-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382927
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382927
    reference: chr 11
allele count: 1
allele frequency: 1.596067290196955e-5
allele num: 62654
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.60C>T
  hgvsp: ENST00000359636.2:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.60C>T
  hgvsp: ENST00000393324.3:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.60C>T
  hgvsp: ENST00000526944.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.60C>T
  hgvsp: ENST00000532471.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.60C>T
  hgvsp: ENST00000526504.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.60C>T
  hgvsp: ENST00000530335.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.81C>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.60C>T
  hgvsp: ENST00000524826.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.60C>T
  hgvsp: ENST00000543262.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.60C>T
  hgvsp: ENST00000526834.1:c.60C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5385
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13965
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4494
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly20Gly
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

11-86382931-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382931
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382931
    reference: chr 11
allele count: 1
allele frequency: 2.335575485799701e-5
allele num: 42816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.56G>A
  hgvsp: ENSP00000433636.1:p.Cys19Tyr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.56G>A
  hgvsp: ENSP00000434690.1:p.Cys19Tyr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.56G>A
  hgvsp: ENSP00000435427.1:p.Cys19Tyr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.56G>A
  hgvsp: ENSP00000376998.2:p.Cys19Tyr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.56G>A
  hgvsp: ENSP00000431182.1:p.Cys19Tyr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.56G>A
  hgvsp: ENSP00000440246.1:p.Cys19Tyr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.77G>A
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.56G>A
  hgvsp: ENSP00000352657.2:p.Cys19Tyr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.56G>A
  hgvsp: ENSP00000434431.1:p.Cys19Tyr
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.56G>A
  hgvsp: ENSP00000437204.1:p.Cys19Tyr
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15542
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6482
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2464
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 869
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Cys19Tyr
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

11-86382932-A-AGGCCC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382932
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382937
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 42794
alternate allele: AGGCCC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.50_54dupGGGCC
  hgvsp: ENSP00000437204.1:p.Cys19GlyfsTer30
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.50_54dupGGGCC
  hgvsp: ENSP00000352657.2:p.Cys19GlyfsTer30
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.71_75dupGGGCC
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.50_54dupGGGCC
  hgvsp: ENSP00000376998.2:p.Cys19GlyfsTer30
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.50_54dupGGGCC
  hgvsp: ENSP00000431182.1:p.Cys19GlyfsTer30
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.50_54dupGGGCC
  hgvsp: ENSP00000435427.1:p.Cys19GlyfsTer30
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.50_54dupGGGCC
  hgvsp: ENSP00000434690.1:p.Cys19GlyfsTer30
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.50_54dupGGGCC
  hgvsp: ENSP00000440246.1:p.Cys19GlyfsTer30
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.50_54dupGGGCC
  hgvsp: ENSP00000433636.1:p.Cys19GlyfsTer30
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.50_54dupGGGCC
  hgvsp: ENSP00000434431.1:p.Cys19GlyfsTer30
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: frameshift
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2434
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6538
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7268
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13546
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1568
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys19GlyfsTer30
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

11-86382937-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382937
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382937
    reference: chr 11
allele count: 1
allele frequency: 3.340236488743403e-5
allele num: 29938
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.50G>A
  hgvsp: ENSP00000440246.1:p.Arg17Gln
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.50G>A
  hgvsp: ENSP00000433636.1:p.Arg17Gln
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.50G>A
  hgvsp: ENSP00000435427.1:p.Arg17Gln
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.50G>A
  hgvsp: ENSP00000434431.1:p.Arg17Gln
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.50G>A
  hgvsp: ENSP00000434690.1:p.Arg17Gln
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.50G>A
  hgvsp: ENSP00000431182.1:p.Arg17Gln
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.50G>A
  hgvsp: ENSP00000376998.2:p.Arg17Gln
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.50G>A
  hgvsp: ENSP00000352657.2:p.Arg17Gln
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.71G>A
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.50G>A
  hgvsp: ENSP00000437204.1:p.Arg17Gln
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7466
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14008
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11073
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4203
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1455
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg17Gln
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

11-86382938-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382938
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382938
    reference: chr 11
allele count: 1
allele frequency: 4.276428327061238e-5
allele num: 23384
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.49C>G
  hgvsp: ENSP00000434431.1:p.Arg17Gly
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.70C>G
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.49C>G
  hgvsp: ENSP00000433636.1:p.Arg17Gly
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.49C>G
  hgvsp: ENSP00000437204.1:p.Arg17Gly
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.49C>G
  hgvsp: ENSP00000434690.1:p.Arg17Gly
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.49C>G
  hgvsp: ENSP00000352657.2:p.Arg17Gly
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.49C>G
  hgvsp: ENSP00000440246.1:p.Arg17Gly
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.49C>G
  hgvsp: ENSP00000431182.1:p.Arg17Gly
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.49C>G
  hgvsp: ENSP00000376998.2:p.Arg17Gly
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.49C>G
  hgvsp: ENSP00000435427.1:p.Arg17Gly
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7723
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9429
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg17Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

11-86382959-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382959
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382959
    reference: chr 11
allele count: 2
allele frequency: 5.211047420531526e-4
allele num: 3838
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.28C>T
  hgvsp: ENSP00000437204.1:p.Arg10Trp
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.28C>T
  hgvsp: ENSP00000435427.1:p.Arg10Trp
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.49C>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.28C>T
  hgvsp: ENSP00000440246.1:p.Arg10Trp
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.28C>T
  hgvsp: ENSP00000352657.2:p.Arg10Trp
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.28C>T
  hgvsp: ENSP00000433636.1:p.Arg10Trp
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.28C>T
  hgvsp: ENSP00000376998.2:p.Arg10Trp
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.28C>T
  hgvsp: ENSP00000434690.1:p.Arg10Trp
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.28C>T
  hgvsp: ENSP00000431182.1:p.Arg10Trp
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.28C>T
  hgvsp: ENSP00000434431.1:p.Arg10Trp
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8850
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg10Trp
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

11-86382960-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382960
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382960
    reference: chr 11
allele count: 1
allele frequency: 2.834467120181406e-4
allele num: 3528
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.27G>A
  hgvsp: ENST00000359636.2:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.27G>A
  hgvsp: ENST00000530335.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.27G>A
  hgvsp: ENST00000526944.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.27G>A
  hgvsp: ENST00000543262.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.27G>A
  hgvsp: ENST00000526504.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.27G>A
  hgvsp: ENST00000532471.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.27G>A
  hgvsp: ENST00000524826.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.27G>A
  hgvsp: ENST00000526834.1:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.27G>A
  hgvsp: ENST00000393324.3:c.27G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.48G>A
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8858
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr9Thr
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-86382975-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382975
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382975
    reference: chr 11
allele count: 161
allele frequency: 8.247950819672131e-2
allele num: 1952
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.12G>T
  hgvsp: ENST00000393324.3:c.12G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.12G>T
  hgvsp: ENST00000524826.1:c.12G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.12G>T
  hgvsp: ENST00000543262.1:c.12G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.33G>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.12G>T
  hgvsp: ENST00000532471.1:c.12G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.12G>T
  hgvsp: ENST00000530335.1:c.12G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.12G>T
  hgvsp: ENST00000526834.1:c.12G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.12G>T
  hgvsp: ENST00000526504.1:c.12G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.12G>T
  hgvsp: ENST00000526944.1:c.12G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.12G>T
  hgvsp: ENST00000359636.2:c.12G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3102
  bin: 7.5e0
  variant carriers: 302
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8304
  bin: 2.5e0
  variant carriers: 113
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 1.25e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 2.75e1
  variant carriers: 13
hgvs: p.Ala4Ala
num of homozygotes: 8
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

11-86382998-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86382998
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86382998
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 918
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.-12C>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.-12C>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.-12C>T
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151376
  ensembl transcript: ENST00000530520
  gene symbol: ME3
  hgvsc: ENST00000530520.1:n.10C>T
  variant of: http://identifiers.org/hgnc/6985
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1618
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8818
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 6.75e1
  variant carriers: 0
hgvs: c.-12C>T
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/11-86383020-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86383020
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86383020
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 274
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000433636
  ensembl transcript: ENST00000526504
  gene symbol: ME3
  hgvsc: ENST00000526504.1:c.-14-20T>G
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000376998
  ensembl transcript: ENST00000393324
  gene symbol: ME3
  hgvsc: ENST00000393324.3:c.-34T>G
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434431
  ensembl transcript: ENST00000526944
  gene symbol: ME3
  hgvsc: ENST00000526944.1:c.-14-20T>G
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000434690
  ensembl transcript: ENST00000530335
  gene symbol: ME3
  hgvsc: ENST00000530335.1:c.-14-20T>G
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000431182
  ensembl transcript: ENST00000524826
  gene symbol: ME3
  hgvsc: ENST00000524826.1:c.-14-20T>G
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000440246
  ensembl transcript: ENST00000543262
  gene symbol: ME3
  hgvsc: ENST00000543262.1:c.-14-20T>G
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000437204
  ensembl transcript: ENST00000526834
  gene symbol: ME3
  hgvsc: ENST00000526834.1:c.-14-20T>G
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000435427
  ensembl transcript: ENST00000532471
  gene symbol: ME3
  hgvsc: ENST00000532471.1:c.-14-20T>G
  variant of: http://identifiers.org/hgnc/6985
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151376
  ensembl protein: ENSP00000352657
  ensembl transcript: ENST00000359636
  gene symbol: ME3
  hgvsc: ENST00000359636.2:c.-14-20T>G
  variant of: http://identifiers.org/hgnc/6985
canonical: false
consequence: 5' UTR
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8516
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

11-86518654-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518654
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518654
    reference: chr 11
allele count: 1
allele frequency: 8.866663120001419e-6
allele num: 112782
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.-13-19C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.-13-19C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+6961C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.-13-19C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+6961C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+6961C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+6961C>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9144
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3454
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5587
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4153
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 772
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22137
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

11-86518654-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518654
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518654
    reference: chr 11
allele count: 2
allele frequency: 1.773332624000284e-5
allele num: 112782
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.-13-19C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+6961C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+6961C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.-13-19C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.-13-19C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+6961C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+6961C>T
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8792
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10080
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2380
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 468
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3955
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2967
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22137
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 4153
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9922
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 394
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

11-86518656-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518656
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518656
    reference: chr 11
allele count: 1
allele frequency: 8.852691218130311e-6
allele num: 112960
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+6963T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.-13-17T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+6963T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+6963T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.-13-17T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.-13-17T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+6963T>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8793
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5589
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3083
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 475
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4155
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2697
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3955
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

11-86518662-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518662
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518662
    reference: chr 11
allele count: 1
allele frequency: 8.833298000141333e-6
allele num: 113208
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.-13-11T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+6969T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+6969T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+6969T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.-13-11T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+6969T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.-13-11T>C
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8804
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3453
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3283
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5589
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22136
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-86518669-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518669
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518669
    reference: chr 11
allele count: 1
allele frequency: 8.808710052499912e-6
allele num: 113524
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+6976A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+6976A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+6976A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.-13-4A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.-13-4A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.-13-4A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+6976A>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9148
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8821
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3453
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3329
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2697
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10171
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3289
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 491
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
hgvs: c.-13-4A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

11-86518676-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518676
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518676
    reference: chr 11
allele count: 2
allele frequency: 1.750363200364075e-5
allele num: 114262
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+6983A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.-10A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+6983A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.-10A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+6983A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+6983A>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8845
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10088
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2408
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3209
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 479
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3453
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3164
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 100
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22134
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3955
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 415
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff

11-86518682-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518682
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518682
    reference: chr 11
allele count: 1
allele frequency: 8.698526469616046e-6
allele num: 114962
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+6989C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.-4C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+6989C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+6989C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.-4C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.-4C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+6989C>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5640
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3955
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10727
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-86518682-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518682
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518682
    reference: chr 11
allele count: 3
allele frequency: 2.609557940884814e-5
allele num: 114962
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+6989C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+6989C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.-4C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.-4C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+6989C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+6989C>T
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3231
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3854
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9149
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2847
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8893
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22134
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 203
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2697
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5640
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 387
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

11-86518683-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518683
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518683
    reference: chr 11
allele count: 3
allele frequency: 2.601817803371956e-5
allele num: 115304
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+6990G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+6990G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.-3G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.-3G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+6990G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+6990G>A
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8909
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10099
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2697
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10815
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

11-86518684-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518684
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518684
    reference: chr 11
allele count: 2
allele frequency: 1.732111617272617e-5
allele num: 115466
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.-2G>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+6991G>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+6991G>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.-2G>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+6991G>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.-2G>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+6991G>T
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9150
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2689
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10101
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8923
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3425
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2748
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4161
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3955
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

11-86518690-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518690
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518690
    reference: chr 11
allele count: 1
allele frequency: 8.585607088277212e-6
allele num: 116474
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.5C>G
  hgvsp: ENSP00000280258.4:p.Ala2Gly
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+6997C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+6997C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+6997C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.5C>G
  hgvsp: ENSP00000435951.1:p.Ala2Gly
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.5C>G
  hgvsp: ENSP00000393015.1:p.Ala2Gly
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+6997C>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3983
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9151
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7944
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2698
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4165
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11337
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 236
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ala2Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/11-86518691-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518691
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518691
    reference: chr 11
allele count: 7
allele frequency: 5.993766482857828e-5
allele num: 116788
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+6998A>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.6A>C
  hgvsp: ENST00000441050.1:c.6A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.6A>C
  hgvsp: ENST00000280258.5:c.6A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+6998A>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+6998A>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+6998A>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.6A>C
  hgvsp: ENST00000527521.1:c.6A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3855
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4094
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9152
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10118
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5636
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5701
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3308
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2208
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala2Ala
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

11-86518695-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518695
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518695
    reference: chr 11
allele count: 5
allele frequency: 4.259596871752058e-5
allele num: 117382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.10A>G
  hgvsp: ENSP00000393015.1:p.Ile4Val
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.10A>G
  hgvsp: ENSP00000280258.4:p.Ile4Val
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.10A>G
  hgvsp: ENSP00000435951.1:p.Ile4Val
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7002A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7002A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7002A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7002A>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 10131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 967
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9147
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1842
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7941
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2407
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4177
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3454
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2698
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 216
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.25e1
  variant carriers: 1
hgvs: p.Ile4Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD

11-86518699-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518699
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518699
    reference: chr 11
allele count: 3
allele frequency: 2.542372881355932e-5
allele num: 118000
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7006C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7006C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.14C>T
  hgvsp: ENSP00000393015.1:p.Pro5Leu
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.14C>T
  hgvsp: ENSP00000435951.1:p.Pro5Leu
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7006C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.14C>T
  hgvsp: ENSP00000280258.4:p.Pro5Leu
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7006C>T
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4695
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9162
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7943
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10161
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2701
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1668
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3455
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5747
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro5Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

11-86518703-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518703
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518703
    reference: chr 11
allele count: 93
allele frequency: 7.833030119264201e-4
allele num: 118728
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7010G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.18G>A
  hgvsp: ENST00000441050.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.18G>A
  hgvsp: ENST00000527521.1:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.18G>A
  hgvsp: ENST00000280258.5:c.18G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7010G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7010G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7010G>A
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1248
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9408
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1560
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7942
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9164
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 693
  bin: 9.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 5036
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3967
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 230
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1362
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3334
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2702
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12766
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gly6Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

11-86518708-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518708
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518708
    reference: chr 11
allele count: 6
allele frequency: 5.024199896166536e-5
allele num: 119422
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7015T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7015T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.23T>G
  hgvsp: ENSP00000435951.1:p.Leu8Arg
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.23T>G
  hgvsp: ENSP00000393015.1:p.Leu8Arg
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7015T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.23T>G
  hgvsp: ENSP00000280258.4:p.Leu8Arg
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7015T>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10208
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5647
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9177
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3865
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 444
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 605
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1561
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7954
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9592
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3465
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu8Arg
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-86518714-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518714
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518714
    reference: chr 11
allele count: 224
allele frequency: 1.865205588955318e-3
allele num: 120094
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7021T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.29T>G
  hgvsp: ENSP00000393015.1:p.Leu10Arg
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7021T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.29T>G
  hgvsp: ENSP00000280258.4:p.Leu10Arg
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.29T>G
  hgvsp: ENSP00000435951.1:p.Leu10Arg
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7021T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7021T>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10249
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2403
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5648
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7955
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3863
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 701
  bin: 9.75e1
  variant carriers: 207
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9737
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 9175
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4195
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3465
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 695
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3970
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2709
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu10Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

11-86518718-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518718
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518718
    reference: chr 11
allele count: 1
allele frequency: 8.30675172780436e-6
allele num: 120384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7025C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7025C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.33C>T
  hgvsp: ENST00000280258.5:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.33C>T
  hgvsp: ENST00000441050.1:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7025C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.33C>T
  hgvsp: ENST00000527521.1:c.33C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7025C>T
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9879
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7981
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10296
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5908
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2716
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14002
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu11Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ

11-86518719-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518719
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518719
    reference: chr 11
allele count: 1
allele frequency: 8.301786544464368e-6
allele num: 120456
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.34T>C
  hgvsp: ENSP00000393015.1:p.Phe12Leu
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.34T>C
  hgvsp: ENSP00000435951.1:p.Phe12Leu
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7026T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.34T>C
  hgvsp: ENSP00000280258.4:p.Phe12Leu
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7026T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7026T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7026T>C
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9900
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10293
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21946
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5925
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3480
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3353
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2717
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Phe12Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-86518720-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518720
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518720
    reference: chr 11
allele count: 1
allele frequency: 8.298617450332775e-6
allele num: 120502
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7027T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.35T>G
  hgvsp: ENSP00000393015.1:p.Phe12Cys
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.35T>G
  hgvsp: ENSP00000280258.4:p.Phe12Cys
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7027T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.35T>G
  hgvsp: ENSP00000435951.1:p.Phe12Cys
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7027T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7027T>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9901
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7982
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2717
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3354
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Phe12Cys
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

11-86518728-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518728
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518728
    reference: chr 11
allele count: 1
allele frequency: 8.272940865018697e-6
allele num: 120876
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7035C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.43C>G
  hgvsp: ENSP00000280258.4:p.Leu15Val
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7035C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7035C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7035C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.43C>G
  hgvsp: ENSP00000435951.1:p.Leu15Val
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.43C>G
  hgvsp: ENSP00000393015.1:p.Leu15Val
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6014
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10053
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9207
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10337
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7990
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3362
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5939
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 290
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2721
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu15Val
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP

11-86518730-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518730
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518730
    reference: chr 11
allele count: 1
allele frequency: 8.267605866693123e-6
allele num: 120954
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7037C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.45C>G
  hgvsp: ENST00000527521.1:c.45C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.45C>G
  hgvsp: ENST00000441050.1:c.45C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7037C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.45C>G
  hgvsp: ENST00000280258.5:c.45C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7037C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7037C>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10350
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5954
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4207
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21941
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3365
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 250
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu15Leu
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

11-86518733-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518733
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518733
    reference: chr 11
allele count: 4
allele frequency: 3.304146704113662e-5
allele num: 121060
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.48T>C
  hgvsp: ENST00000441050.1:c.48T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.48T>C
  hgvsp: ENST00000280258.5:c.48T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7040T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7040T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7040T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.48T>C
  hgvsp: ENST00000527521.1:c.48T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7040T>C
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10135
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3989
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4212
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Cys16Cys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

11-86518740-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518740
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518740
    reference: chr 11
allele count: 1
allele frequency: 8.251914444151043e-6
allele num: 121184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.55G>A
  hgvsp: ENSP00000393015.1:p.Gly19Arg
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7047G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.55G>A
  hgvsp: ENSP00000435951.1:p.Gly19Arg
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7047G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7047G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.55G>A
  hgvsp: ENSP00000280258.4:p.Gly19Arg
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7047G>A
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2416
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10197
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2723
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3484
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly19Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS

11-86518746-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518746
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518746
    reference: chr 11
allele count: 4
allele frequency: 3.299295600389317e-5
allele num: 121238
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.61G>A
  hgvsp: ENSP00000280258.4:p.Val21Met
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.61G>A
  hgvsp: ENSP00000435951.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7053G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7053G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7053G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.61G>A
  hgvsp: ENSP00000393015.1:p.Val21Met
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7053G>A
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6072
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 493
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3984
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14792
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4214
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2723
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Val21Met
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

11-86518753-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518753
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518753
    reference: chr 11
allele count: 5
allele frequency: 4.122963256151461e-5
allele num: 121272
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.68C>T
  hgvsp: ENSP00000435951.1:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.68C>T
  hgvsp: ENSP00000393015.1:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7060C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.68C>T
  hgvsp: ENSP00000280258.4:p.Pro23Leu
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7060C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7060C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7060C>T
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6062
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10274
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3985
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Pro23Leu
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum

11-86518754-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518754
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518754
    reference: chr 11
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.69T>A
  hgvsp: ENST00000280258.5:c.69T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7061T>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7061T>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.69T>A
  hgvsp: ENST00000441050.1:c.69T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7061T>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.69T>A
  hgvsp: ENST00000527521.1:c.69T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7061T>A
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10395
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10279
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4211
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14859
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3985
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Pro23Pro
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-86518756-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518756
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518756
    reference: chr 11
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.71A>G
  hgvsp: ENSP00000393015.1:p.Tyr24Cys
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.71A>G
  hgvsp: ENSP00000435951.1:p.Tyr24Cys
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7063A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7063A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7063A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.71A>G
  hgvsp: ENSP00000280258.4:p.Tyr24Cys
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7063A>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9212
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10283
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3985
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4212
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21935
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14862
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Tyr24Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

11-86518760-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518760
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518760
    reference: chr 11
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7067T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.75T>C
  hgvsp: ENST00000527521.1:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.75T>C
  hgvsp: ENST00000441050.1:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7067T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7067T>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.75T>C
  hgvsp: ENST00000280258.5:c.75T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7067T>C
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 487
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10400
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 294
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2723
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6010
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14878
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser25Ser
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-86518772-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518772
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518772
    reference: chr 11
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7079A>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.87A>C
  hgvsp: ENSP00000280258.4:p.Lys29Asn
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.87A>C
  hgvsp: ENSP00000435951.1:p.Lys29Asn
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7079A>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.87A>C
  hgvsp: ENSP00000393015.1:p.Lys29Asn
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7079A>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7079A>C
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10405
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7991
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14929
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3484
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21933
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6022
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3984
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Lys29Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD

11-86518790-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518790
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518790
    reference: chr 11
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7097C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.105C>T
  hgvsp: ENST00000280258.5:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7097C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.105C>T
  hgvsp: ENST00000527521.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7097C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.105C>T
  hgvsp: ENST00000441050.1:c.105C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7097C>T
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6089
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4210
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3379
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Tyr35Tyr
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

11-86518791-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518791
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518791
    reference: chr 11
allele count: 13
allele frequency: 1.070787275752434e-4
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7098C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7098C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7098C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.106C>T
  hgvsp: ENSP00000280258.4:p.Arg36Cys
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.106C>T
  hgvsp: ENSP00000393015.1:p.Arg36Cys
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.106C>T
  hgvsp: ENSP00000435951.1:p.Arg36Cys
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7098C>T
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5677
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6087
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3883
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 491
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 10407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7990
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14936
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6025
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg36Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

11-86518792-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518792
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518792
    reference: chr 11
allele count: 2
allele frequency: 1.647392178181938e-5
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.107G>A
  hgvsp: ENSP00000435951.1:p.Arg36His
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7099G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.107G>A
  hgvsp: ENSP00000280258.4:p.Arg36His
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7099G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.107G>A
  hgvsp: ENSP00000393015.1:p.Arg36His
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7099G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7099G>A
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9208
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3484
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2724
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg36His
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-86518799-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518799
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518799
    reference: chr 11
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.114T>G
  hgvsp: ENST00000527521.1:c.114T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.114T>G
  hgvsp: ENST00000441050.1:c.114T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7106T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7106T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.114T>G
  hgvsp: ENST00000280258.5:c.114T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7106T>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7106T>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3380
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6026
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro38Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum

11-86518802-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518802
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518802
    reference: chr 11
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7109C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.117C>T
  hgvsp: ENST00000441050.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.117C>T
  hgvsp: ENST00000527521.1:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7109C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7109C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.117C>T
  hgvsp: ENST00000280258.5:c.117C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7109C>T
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10413
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7991
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14937
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2723
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3484
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4210
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val39Val
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

11-86518803-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518803
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518803
    reference: chr 11
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7110G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.118G>A
  hgvsp: ENSP00000435951.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7110G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.118G>A
  hgvsp: ENSP00000393015.1:p.Val40Ile
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7110G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7110G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.118G>A
  hgvsp: ENSP00000280258.4:p.Val40Ile
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7992
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5679
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10414
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14939
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3983
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Val40Ile
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

11-86518810-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518810
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518810
    reference: chr 11
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7117C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.125C>G
  hgvsp: ENSP00000280258.4:p.Pro42Arg
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.125C>G
  hgvsp: ENSP00000393015.1:p.Pro42Arg
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7117C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7117C>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.125C>G
  hgvsp: ENSP00000435951.1:p.Pro42Arg
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7117C>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7994
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6085
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5678
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21927
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3379
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4210
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3982
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro42Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

11-86518814-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518814
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518814
    reference: chr 11
allele count: 3
allele frequency: 2.471088267272907e-5
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.129G>T
  hgvsp: ENSP00000280258.4:p.Gln43His
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.129G>T
  hgvsp: ENSP00000393015.1:p.Gln43His
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7121G>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.129G>T
  hgvsp: ENSP00000435951.1:p.Gln43His
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7121G>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7121G>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7121G>T
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10345
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21927
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Gln43His
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

11-86518818-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518818
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518818
    reference: chr 11
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7125A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.133A>G
  hgvsp: ENSP00000280258.4:p.Thr45Ala
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7125A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.133A>G
  hgvsp: ENSP00000435951.1:p.Thr45Ala
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.133A>G
  hgvsp: ENSP00000393015.1:p.Thr45Ala
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7125A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7125A>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10412
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3886
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5675
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3382
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6028
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4211
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr45Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
reference allele: A
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

11-86518824-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518824
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518824
    reference: chr 11
allele count: 2
allele frequency: 1.647365039619129e-5
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7131A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.139A>G
  hgvsp: ENSP00000393015.1:p.Asn47Asp
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.139A>G
  hgvsp: ENSP00000280258.4:p.Asn47Asp
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7131A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7131A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7131A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.139A>G
  hgvsp: ENSP00000435951.1:p.Asn47Asp
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 10410
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9209
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3885
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3984
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21923
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn47Asp
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum

11-86518825-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518825
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518825
    reference: chr 11
allele count: 5
allele frequency: 4.118412599047823e-5
allele num: 121406
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7132A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.140A>G
  hgvsp: ENSP00000393015.1:p.Asn47Ser
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.140A>G
  hgvsp: ENSP00000280258.4:p.Asn47Ser
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.140A>G
  hgvsp: ENSP00000435951.1:p.Asn47Ser
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7132A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7132A>G
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7132A>G
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10411
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5674
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6028
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14923
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn47Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

11-86518830-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518830
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518830
    reference: chr 11
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7137G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7137G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.145G>A
  hgvsp: ENSP00000435951.1:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.144+1G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.145G>A
  hgvsp: ENSP00000280258.4:p.Ala49Thr
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7137G>A
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7137G>A
  variant of: http://identifiers.org/hgnc/14370
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10418
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2723
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3484
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4211
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6025
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: c.144+1G>A
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/11-86518833-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518833
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518833
    reference: chr 11
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.148A>C
  hgvsp: ENSP00000280258.4:p.Lys50Gln
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.148A>C
  hgvsp: ENSP00000435951.1:p.Lys50Gln
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7140A>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7140A>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.144+4A>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7140A>C
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7140A>C
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7996
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6084
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10342
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2723
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3381
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys50Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ

11-86518841-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518841
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518841
    reference: chr 11
allele count: 1
allele frequency: 8.236960890909689e-6
allele num: 121404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7148C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.156C>T
  hgvsp: ENST00000280258.5:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7148C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7148C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.156C>T
  hgvsp: ENST00000527521.1:c.156C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7148C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.144+12C>T
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3884
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10351
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7995
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2414
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3383
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4209
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14918
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp52Asp
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

11-86518850-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 86518850
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 86518850
    reference: chr 11
allele count: 7
allele frequency: 5.765967611736215e-5
allele num: 121402
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000436676
  ensembl transcript: ENST00000532234
  gene symbol: PRSS23
  hgvsc: ENST00000532234.1:c.-12+7157C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000437268
  ensembl transcript: ENST00000533902
  gene symbol: PRSS23
  hgvsc: ENST00000533902.2:c.-12+7157C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000435951
  ensembl transcript: ENST00000527521
  gene symbol: PRSS23
  hgvsc: ENST00000527521.1:c.165C>T
  hgvsp: ENST00000527521.1:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000533880
  gene symbol: PRSS23
  hgvsc: ENST00000533880.1:n.108+7157C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000280258
  ensembl transcript: ENST00000280258
  gene symbol: PRSS23
  hgvsc: ENST00000280258.5:c.165C>T
  hgvsp: ENST00000280258.5:c.165C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl transcript: ENST00000531475
  gene symbol: PRSS23
  hgvsc: ENST00000531475.1:n.108+7157C>T
  variant of: http://identifiers.org/hgnc/14370
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000150687
  ensembl protein: ENSP00000393015
  ensembl transcript: ENST00000441050
  gene symbol: PRSS23
  hgvsc: ENST00000441050.1:c.144+21C>T
  variant of: http://identifiers.org/hgnc/14370
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10349
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7997
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5676
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala55Ala
num of homozygotes: 0
reference allele: C

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

GenotypeQuality
all individuals: 312
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 50444
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 205
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5099
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 270
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2499
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 21
bin: 8.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545547278291243e-5
allele num: 64702
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16326
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8496
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.394283e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.813e0

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 1.109e0

MQRankSum
type: SiteQuality
SIO_000300: -1.52e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 1.287e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.19e-1

GenotypeQuality
all individuals: 3336
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 284
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4962
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49091
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 393
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 98
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9584
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6402
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8464
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.236746912810279e-5
allele num: 64136
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16188
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.985e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.376857e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.2e0

QD
type: SiteQuality
SIO_000300: 1.292e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-3

GenotypeQuality
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8261
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4158
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 758
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1717
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42042
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 73
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 1.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.209774981853375e-4
allele num: 8266
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11120
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.811e0

VQSLOD
type: SiteQuality
SIO_000300: -5.792e-1

MQ
type: SiteQuality
SIO_000300: 5.849e1

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

DP
type: SiteQuality
SIO_000300: 1.274315e6

ClippingRankSum
type: SiteQuality
SIO_000300: -6.97e-1

QD
type: SiteQuality
SIO_000300: 1.237e1

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

GenotypeQuality
all individuals: 4158
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 126
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1717
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 622
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8261
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1096
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 42042
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.623587478893363e-5
allele num: 61592
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15364
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 808
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8780
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8266
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.37e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.97e-1

FS
type: SiteQuality
SIO_000300: 3.811e0

MQRankSum
type: SiteQuality
SIO_000300: -2.2e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.792e-1

QD
type: SiteQuality
SIO_000300: 1.237e1

DP
type: SiteQuality
SIO_000300: 1.274315e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.41e-1

MQ
type: SiteQuality
SIO_000300: 5.849e1

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 345
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1374
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2026
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 9956
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39737
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3883
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5998
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11054
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.276432620163167e-5
allele num: 61042
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.25e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.31e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.244628e6

QD
type: SiteQuality
SIO_000300: 1.313e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-1

FS
type: SiteQuality
SIO_000300: 2.125e0

GenotypeQuality
all individuals: 6
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 212
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 581
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3883
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 952
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1374
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9956
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2026
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39737
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11054
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 796
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5998
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.638216310081583e-5
allele num: 61042
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.31e-1

DP
type: SiteQuality
SIO_000300: 1.244628e6

VQSLOD
type: SiteQuality
SIO_000300: 8.35e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQRankSum
type: SiteQuality
SIO_000300: -5.25e-1

FS
type: SiteQuality
SIO_000300: 2.125e0

QD
type: SiteQuality
SIO_000300: 1.313e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 558
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1662
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1133
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2293
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3755
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 37364
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8142
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10988
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.654478673769895e-5
allele num: 60442
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8482
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 786
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5928
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.08e-1

InbreedingCoeff
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MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: -2.12e-1

ClippingRankSum
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SIO_000300: -7.000000000000001e-2

QD
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VQSLOD
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SIO_000300: 2.2e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.665e0

DP
type: SiteQuality
SIO_000300: 1.21663e6

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8332
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8078
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 9.170946441672781e-5
allele num: 10904
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
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FS
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SIO_000300: 0.0e0

ReadPosRankSum
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SIO_000300: 1.13e0

VQSLOD
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DP
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MQ
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QD
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SIO_000300: 1.802e1

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7826
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7788
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10582
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5572
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14196
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.749597592553713e-5
allele num: 57156
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.42e0

MQRankSum
type: SiteQuality
SIO_000300: 4.08e-1

ReadPosRankSum
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SIO_000300: 2.37e0

VQSLOD
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SIO_000300: 1.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
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SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -2.475e0

DP
type: SiteQuality
SIO_000300: 1.043015e6

QD
type: SiteQuality
SIO_000300: 1.095e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.5e-3

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 634
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.466705778820769e-4
allele num: 6818
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11950
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.22e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.43411e5

ReadPosRankSum
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SIO_000300: 1.04e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.57e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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SIO_000300: -9.03e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.125e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e-1

QD
type: SiteQuality
SIO_000300: 1.661e1

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 1
allele frequency: 1.105705440070765e-4
allele num: 9044
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6818
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11950
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 49432
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4554
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6444
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Other
type: Population
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allele frequency: 0.0e0
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InbreedingCoeff
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SIO_000300: 1.57e-2

BaseQRankSum
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SIO_000300: 1.22e0

VQSLOD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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MQ
type: SiteQuality
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QD
type: SiteQuality
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FS
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SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 8.43411e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 6442
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9042
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11816
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.031446796408402e-5
allele num: 49226
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4478
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East Asian
type: Population
allele count: 1
allele frequency: 1.471886959081543e-4
allele num: 6794
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Other
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ClippingRankSum
type: SiteQuality
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQ
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FS
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DP
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MQRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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allele num: 9042
num of homozygotes: 0

South Asian
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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East Asian
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Other
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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FS
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ReadPosRankSum
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DP
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 2.214348981399469e-4
allele num: 9032
num of homozygotes: 0

African
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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East Asian
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Other
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VQSLOD
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MQRankSum
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BaseQRankSum
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FS
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ClippingRankSum
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QD
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InbreedingCoeff
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DP
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MQ
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Latino
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Other
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African
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DP
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InbreedingCoeff
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FS
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ClippingRankSum
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QD
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MQ
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Non-Finnish)
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Latino
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South Asian
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African
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Other
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European (Finnish)
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ClippingRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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FS
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ReadPosRankSum
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MQRankSum
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QD
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DP
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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Latino
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South Asian
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European (Finnish)
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African
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East Asian
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European (Non-Finnish)
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DP
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MQ
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ReadPosRankSum
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QD
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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South Asian
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African
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Latino
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ClippingRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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FS
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ReadPosRankSum
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MQRankSum
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VQSLOD
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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European (Non-Finnish)
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Other
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South Asian
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African
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FS
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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MQ
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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Other
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European (Non-Finnish)
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European (Finnish)
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South Asian
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African
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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FS
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DP
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BaseQRankSum
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MQ
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VQSLOD
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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Other
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East Asian
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South Asian
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Latino
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European (Finnish)
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InbreedingCoeff
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ClippingRankSum
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FS
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VQSLOD
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BaseQRankSum
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MQRankSum
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DP
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MQ
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QD
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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Other
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Latino
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allele frequency: 0.0e0
allele num: 156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 370
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 240
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

QD
type: SiteQuality
SIO_000300: 1.583e1

VQSLOD
type: SiteQuality
SIO_000300: -1.244e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.94e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.55e-1

DP
type: SiteQuality
SIO_000300: 8.4191e4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeQuality
all individuals: 9097
bin: 7.5e0
variant carriers: 0

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

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

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 206
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 298
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 134
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1434
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 9.328358208955224e-4
allele num: 1072
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 8.0295e4

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.659999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 9.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e0

QD
type: SiteQuality
SIO_000300: 1.838e1

VQSLOD
type: SiteQuality
SIO_000300: -2.092e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.93e-2

GenotypeQuality
all individuals: 29
bin: 5.75e1
variant carriers: 25

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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bin: 4.25e1
variant carriers: 5

GenotypeQuality
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variant carriers: 45

GenotypeQuality
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bin: 1.75e1
variant carriers: 64

GenotypeQuality
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variant carriers: 16

GenotypeQuality
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bin: 7.75e1
variant carriers: 15

GenotypeQuality
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variant carriers: 49

GenotypeQuality
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GenotypeQuality
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variant carriers: 12

GenotypeQuality
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variant carriers: 24

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 20

GenotypeQuality
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bin: 8.75e1
variant carriers: 20

GenotypeQuality
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bin: 5.25e1
variant carriers: 15

GenotypeQuality
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variant carriers: 140

GenotypeQuality
all individuals: 28
bin: 4.75e1
variant carriers: 20

GenotypeQuality
all individuals: 15
bin: 8.25e1
variant carriers: 14

Other
type: Population
allele count: 1
allele frequency: 3.125e-2
allele num: 32
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.666666666666667e-2
allele num: 120
num of homozygotes: 0

South Asian
type: Population
allele count: 47
allele frequency: 5.994897959183673e-2
allele num: 784
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 15
allele frequency: 8.064516129032258e-2
allele num: 186
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 70
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 4.054054054054054e-2
allele num: 74
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 93
allele frequency: 1.355685131195335e-1
allele num: 686
num of homozygotes: 6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

DP
type: SiteQuality
SIO_000300: 5.6993e4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

QD
type: SiteQuality
SIO_000300: 1.741e1

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 444
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 266
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 18
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.73e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.54e0

QD
type: SiteQuality
SIO_000300: 5.98e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.9355e4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.537e0

VQSLOD
type: SiteQuality
SIO_000300: -3.392e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.537e0

GenotypeQuality
all individuals: 104
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1745
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 0
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GenotypeQuality
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GenotypeQuality
all individuals: 12
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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: 0
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 82
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 22
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 102
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.516e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 9.460000000000001e0

DP
type: SiteQuality
SIO_000300: 2.7646e4

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.78e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3955
bin: 8.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.165229550221394e-4
allele num: 8582
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64564
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.58e-1

FS
type: SiteQuality
SIO_000300: 5.001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 2.04e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.332e0

DP
type: SiteQuality
SIO_000300: 2.313467e6

MQ
type: SiteQuality
SIO_000300: 5.917e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

QD
type: SiteQuality
SIO_000300: 1.293e1

GenotypeQuality
all individuals: 5587
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 21
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2697
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variant carriers: 0

GenotypeQuality
all individuals: 3288
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8582
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.915341888527102e-4
allele num: 10442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10258
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64564
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.917e1

FS
type: SiteQuality
SIO_000300: 5.001e0

DP
type: SiteQuality
SIO_000300: 2.313467e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.332e0

MQRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: 2.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

QD
type: SiteQuality
SIO_000300: 1.293e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9955
bin: 6.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 818
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10550
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.547269070091289e-5
allele num: 64630
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.43e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.47e-1

FS
type: SiteQuality
SIO_000300: 1.122e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.3e-2

DP
type: SiteQuality
SIO_000300: 2.314335e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.983e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.359999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: 1.84e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 177
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GenotypeQuality
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.733307377846993e-5
allele num: 10274
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10708
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64700
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.317005e6

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 9.64e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.28e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

FS
type: SiteQuality
SIO_000300: 2.285e0

QD
type: SiteQuality
SIO_000300: 1.186e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.71e0

GenotypeQuality
all individuals: 68
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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
all individuals: 413
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variant carriers: 0

GenotypeQuality
all individuals: 52
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64772
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.72762645914397e-5
allele num: 10280
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 822
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: 11508
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10942
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.31e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.13e-1

QD
type: SiteQuality
SIO_000300: 6.83e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e0

MQRankSum
type: SiteQuality
SIO_000300: -8.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.27e0

DP
type: SiteQuality
SIO_000300: 2.320486e6

GenotypeQuality
all individuals: 282
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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
all individuals: 75
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4160
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 191
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5619
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 824
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.742767514813524e-4
allele num: 11476
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11518
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: 0
allele frequency: 0.0e0
allele num: 64942
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.97e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

DP
type: SiteQuality
SIO_000300: 2.325996e6

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.6e-2

FS
type: SiteQuality
SIO_000300: 2.604e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.82e0

QD
type: SiteQuality
SIO_000300: 1.078e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2874
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
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
all individuals: 3454
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4160
bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65094
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.350033400133601e-5
allele num: 11976
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

FS
type: SiteQuality
SIO_000300: 3.304e0

QD
type: SiteQuality
SIO_000300: 1.183e1

MQRankSum
type: SiteQuality
SIO_000300: 9.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.0e-3

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 2.33322e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

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

GenotypeQuality
all individuals: 3454
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4160
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3291
bin: 7.25e1
variant carriers: 1

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: 11522
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.160900859066636e-4
allele num: 8614
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.67000668002672e-4
allele num: 11976
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65094
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 8.74e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 9.77e-1

FS
type: SiteQuality
SIO_000300: 3.304e0

QD
type: SiteQuality
SIO_000300: 1.183e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

DP
type: SiteQuality
SIO_000300: 2.33322e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

GenotypeQuality
all individuals: 72
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3292
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4161
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2802
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22132
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3954
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12226
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.603203829865586e-5
allele num: 65172
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 5.679999999999999e-1

QD
type: SiteQuality
SIO_000300: 9.76e0

FS
type: SiteQuality
SIO_000300: 1.145e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.2e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.13e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

DP
type: SiteQuality
SIO_000300: 2.334895e6

GenotypeQuality
all individuals: 10926
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22131
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 221
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5660
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2698
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3293
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12340
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.201923076923077e-3
allele num: 832
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.533460099368214e-5
allele num: 65212
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11528
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.69e-1

QD
type: SiteQuality
SIO_000300: 1.195e1

FS
type: SiteQuality
SIO_000300: 3.245e0

DP
type: SiteQuality
SIO_000300: 2.336169e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.543e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.29e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.7e-2

MQ
type: SiteQuality
SIO_000300: 5.938e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.98e-1

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

GenotypeQuality
all individuals: 323
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variant carriers: 0

GenotypeQuality
all individuals: 2276
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variant carriers: 0

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
all individuals: 355
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variant carriers: 0

GenotypeQuality
all individuals: 117
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GenotypeQuality
all individuals: 22129
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5686
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3298
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527790509365356e-5
allele num: 65454
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13056
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8626
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.109e0

VQSLOD
type: SiteQuality
SIO_000300: 8.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.77e0

DP
type: SiteQuality
SIO_000300: 2.346822e6

MQ
type: SiteQuality
SIO_000300: 5.909e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.7e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.97e-1

QD
type: SiteQuality
SIO_000300: 1.006e1

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22128
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 11570
bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2698
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 7
allele frequency: 6.765899864682003e-4
allele num: 10346
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65540
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13268
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.349157e6

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.86e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.789e0

FS
type: SiteQuality
SIO_000300: 1.769e0

MQRankSum
type: SiteQuality
SIO_000300: 4.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.58e0

QD
type: SiteQuality
SIO_000300: 1.252e1

GenotypeQuality
all individuals: 106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 111
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.614754348024733e-5
allele num: 65662
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: 868
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: 8644
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13712
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.812e0

MQ
type: SiteQuality
SIO_000300: 5.818e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.15e0

VQSLOD
type: SiteQuality
SIO_000300: -2.117e1

FS
type: SiteQuality
SIO_000300: 6.1735e1

DP
type: SiteQuality
SIO_000300: 2.354049e6

MQRankSum
type: SiteQuality
SIO_000300: -4.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.952e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

QD
type: SiteQuality
SIO_000300: 2.7e-1

GenotypeQuality
all individuals: 3314
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 2.5e0
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GenotypeQuality
all individuals: 83
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GenotypeQuality
all individuals: 22103
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
all individuals: 86
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GenotypeQuality
all individuals: 12290
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GenotypeQuality
all individuals: 4180
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.469010175763182e-4
allele num: 8648
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65822
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.359246e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.858e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.41e0

MQRankSum
type: SiteQuality
SIO_000300: -1.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

MQ
type: SiteQuality
SIO_000300: 5.946e1

QD
type: SiteQuality
SIO_000300: 1.216e1

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5790
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3457
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4185
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22100
bin: 9.75e1
variant carriers: 93

European (Non-Finnish)
type: Population
allele count: 72
allele frequency: 1.090545575717185e-3
allele num: 66022
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 21
allele frequency: 3.175083156939824e-3
allele num: 6614
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: 14636
num of homozygotes: 0

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 5.51e0

MQRankSum
type: SiteQuality
SIO_000300: 4.05e-1

QD
type: SiteQuality
SIO_000300: 1.288e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.52e-1

MQ
type: SiteQuality
SIO_000300: 5.955e1

DP
type: SiteQuality
SIO_000300: 2.371287e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.3e0

GenotypeQuality
all individuals: 5826
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2707
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 189
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22054
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 3967
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3335
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4192
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13202
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15098
num of homozygotes: 0

African
type: Population
allele count: 6
allele frequency: 5.779233288383741e-4
allele num: 10382
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
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: 0
allele frequency: 0.0e0
allele num: 66226
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 3.85e0

QD
type: SiteQuality
SIO_000300: 1.181e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.93e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 2.368218e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-1

MQ
type: SiteQuality
SIO_000300: 5.977e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.1e-3

GenotypeQuality
all individuals: 13
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 136
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3339
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5862
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22060
bin: 9.75e1
variant carriers: 224

GenotypeQuality
all individuals: 13735
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 9
allele frequency: 8.657175836860331e-4
allele num: 10396
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 202
allele frequency: 3.04244359430069e-3
allele num: 66394
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 6
allele frequency: 9.071666162685213e-4
allele num: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

South Asian
type: Population
allele count: 3
allele frequency: 1.927277399460362e-4
allele num: 15566
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.79e-1

DP
type: SiteQuality
SIO_000300: 2.387541e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.25e-1

QD
type: SiteQuality
SIO_000300: 1.254e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.4e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
all individuals: 14
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 110
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3480
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3353
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4202
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variant carriers: 0

GenotypeQuality
all individuals: 83
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variant carriers: 0

GenotypeQuality
all individuals: 21945
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3983
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66458
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.336332530731213e-5
allele num: 15782
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: 10400
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.213e0

MQRankSum
type: SiteQuality
SIO_000300: 3.1e-1

QD
type: SiteQuality
SIO_000300: 1.394e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.661e0

DP
type: SiteQuality
SIO_000300: 2.366593e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

GenotypeQuality
all individuals: 83
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 60
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14098
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
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variant carriers: 0

GenotypeQuality
all individuals: 3989
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
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variant carriers: 0

GenotypeQuality
all individuals: 4204
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 3.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 898
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: 10400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504392827055001e-5
allele num: 66472
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -4.467e-1

DP
type: SiteQuality
SIO_000300: 2.367197e6

MQ
type: SiteQuality
SIO_000300: 5.945e1

MQRankSum
type: SiteQuality
SIO_000300: -8.179999999999999e-1

QD
type: SiteQuality
SIO_000300: 1.519e1

FS
type: SiteQuality
SIO_000300: 2.099e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.102e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5930
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21945
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3988
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3481
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
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variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14102
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
all individuals: 4204
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15872
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.367701e6

VQSLOD
type: SiteQuality
SIO_000300: 1.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e0

FS
type: SiteQuality
SIO_000300: 1.837e0

MQ
type: SiteQuality
SIO_000300: 5.96e1

QD
type: SiteQuality
SIO_000300: 1.26e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.214e0

GenotypeQuality
all individuals: 21944
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 24
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 4206
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 3482
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
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variant carriers: 0

GenotypeQuality
all individuals: 3984
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14500
bin: 6.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502087902184036e-5
allele num: 66574
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16152
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.62e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.347e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 6.59e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.375e0

DP
type: SiteQuality
SIO_000300: 2.372972e6

GenotypeQuality
all individuals: 24
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2721
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variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14563
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variant carriers: 0

GenotypeQuality
all individuals: 3481
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3983
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16208
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: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501636784094663e-5
allele num: 66594
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.111e0

VQSLOD
type: SiteQuality
SIO_000300: -1.771e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e0

FS
type: SiteQuality
SIO_000300: 5.616e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -9.79e-1

DP
type: SiteQuality
SIO_000300: 2.374119e6

MQRankSum
type: SiteQuality
SIO_000300: -1.188e0

QD
type: SiteQuality
SIO_000300: 1.297e1

GenotypeQuality
all individuals: 5979
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 3370
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variant carriers: 0

GenotypeQuality
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 14669
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variant carriers: 0

GenotypeQuality
all individuals: 21939
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 3483
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.003842459173871e-5
allele num: 66624
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16282
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: -6.18e-1

FS
type: SiteQuality
SIO_000300: 5.54e-1

DP
type: SiteQuality
SIO_000300: 2.375024e6

VQSLOD
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

QD
type: SiteQuality
SIO_000300: 1.065e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.602e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.7e-1

GenotypeQuality
all individuals: 3984
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5988
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3372
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4213
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21939
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14740
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
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African
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Other
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Latino
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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South Asian
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ReadPosRankSum
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DP
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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MQ
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MQRankSum
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ClippingRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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East Asian
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

FS
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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DP
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VQSLOD
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BaseQRankSum
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MQ
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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African
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allele num: 10404
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South Asian
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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East Asian
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MQRankSum
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VQSLOD
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QD
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele num: 10404
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European (Non-Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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East Asian
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FS
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DP
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MQ
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MQRankSum
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QD
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.149e0

ReadPosRankSum
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SIO_000300: 1.24e0

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

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

FS
type: SiteQuality
SIO_000300: 2.319e0

MQRankSum
type: SiteQuality
SIO_000300: 2.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.12e-1

VQSLOD
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QD
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DP
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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MQ
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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allele frequency: 0.0e0
allele num: 11578
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
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allele num: 66716
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European (Finnish)
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South Asian
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MQRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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DP
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FS
type: SiteQuality
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QD
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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East Asian
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Latino
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European (Non-Finnish)
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Other
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ReadPosRankSum
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InbreedingCoeff
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DP
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MQ
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FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele num: 8654
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Other
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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African
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MQRankSum
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ReadPosRankSum
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FS
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MQ
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ClippingRankSum
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DP
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InbreedingCoeff
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QD
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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East Asian
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African
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European (Finnish)
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Latino
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Other
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MQ
type: SiteQuality
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FS
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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European (Finnish)
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Latino
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Other
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African
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European (Non-Finnish)
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South Asian
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MQRankSum
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ClippingRankSum
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DP
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VQSLOD
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QD
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MQ
type: SiteQuality
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InbreedingCoeff
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FS
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.31e-1

BaseQRankSum
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SIO_000300: 6.73e-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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East Asian
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allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

ReadPosRankSum
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QD
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DP
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InbreedingCoeff
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MQ
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.127e0

ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 1.727414061150458e-4
allele num: 11578
num of homozygotes: 0

African
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66736
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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QD
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ClippingRankSum
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MQ
type: SiteQuality
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MQRankSum
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FS
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SIO_000300: 1.093e0

DP
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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SIO_000300: 1.05e0

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

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

InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
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SIO_000300: 5.991e1

VQSLOD
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BaseQRankSum
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ClippingRankSum
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SIO_000300: -3.58e-1

FS
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SIO_000300: 3.194e0

MQRankSum
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QD
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DP
type: SiteQuality
SIO_000300: 2.378015e6

ReadPosRankSum
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SIO_000300: 1.76e0

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

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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African
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allele frequency: 0.0e0
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FS
type: SiteQuality
SIO_000300: 1.58e0

BaseQRankSum
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SIO_000300: -1.433e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.158e0

MQ
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 8.51e-1

InbreedingCoeff
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DP
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SIO_000300: 2.377912e6

VQSLOD
type: SiteQuality
SIO_000300: 3.22e-1

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

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

African
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allele count: 3
allele frequency: 2.884060757546626e-4
allele num: 10402
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Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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South Asian
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

InbreedingCoeff
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ClippingRankSum
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MQ
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SIO_000300: 6.0e1

DP
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FS
type: SiteQuality
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VQSLOD
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MQRankSum
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BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 1.094e1

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

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

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

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

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

African
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Other
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
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Latino
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allele num: 11578
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South Asian
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East Asian
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InbreedingCoeff
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MQ
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VQSLOD
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FS
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ClippingRankSum
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BaseQRankSum
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QD
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DP
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ReadPosRankSum
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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allele frequency: 7.492208103572285e-5
allele num: 66736
num of homozygotes: 0

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

African
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allele num: 10404
num of homozygotes: 0

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

GenotypeQuality
all individuals: 14938
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4209
bin: 7.75e1
variant carriers: 0

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

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

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

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -2.06e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.48e0

QD
type: SiteQuality
SIO_000300: 1.635e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.5e0

FS
type: SiteQuality
SIO_000300: 4.038e0

MQRankSum
type: SiteQuality
SIO_000300: 8.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.376917e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.628e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 12
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3986
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21915
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 10
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3484
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2723
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6021
bin: 6.75e1
variant carriers: 0

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

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

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

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

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.17e-1

DP
type: SiteQuality
SIO_000300: 2.376787e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.243e0

QD
type: SiteQuality
SIO_000300: 1.583e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.74e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4