11-82561162-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561162
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561162
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 2188
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.657-49A>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.279-49A>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.279-49A>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.279-49A>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.594-49A>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.279-49A>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.279-49A>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.471-49A>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.279-49A>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.279-49A>T
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11711
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 919
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5925
  bin: 7.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: DP
site quality: QD

11-82561317-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561317
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561317
    reference: chr 11
allele count: 1
allele frequency: 9.023479092598943e-6
allele num: 110822
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.278+49G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.278+49G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.278+49G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.656+49G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.278+49G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.278+49G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.278+49G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.470+49G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.593+49G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.278+49G>C
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10166
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3504
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8119
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2194
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1489
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1757
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4236
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3392
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2588
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1187
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2285
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 17407
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1600
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: C
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS

http://identifiers.org/exac.variant/11-82561328-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561328
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561328
    reference: chr 11
allele count: 2
allele frequency: 1.80092567579736e-5
allele num: 111054
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.593+38G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.278+38G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.278+38G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.278+38G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.278+38G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.278+38G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.656+38G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.278+38G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.278+38G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.470+38G>T
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4243
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3558
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 751
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2593
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10485
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1744
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7234
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 773
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1195
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2798
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum

11-82561338-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561338
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561338
    reference: chr 11
allele count: 5
allele frequency: 4.484948512791073e-5
allele num: 111484
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.278+28G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.278+28G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.278+28G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.278+28G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.278+28G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.278+28G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.470+28G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.656+28G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.278+28G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.593+28G>A
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11904
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3819
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10865
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4253
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 949
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 5.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2388
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 552
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum

11-82561339-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561339
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561339
    reference: chr 11
allele count: 25791
allele frequency: 2.279686036028073e-1
allele num: 113134
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.278+27C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.278+27C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.278+27C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.278+27C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.593+27C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.278+27C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.470+27C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.656+27C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.278+27C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.278+27C>T
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.75e1
  variant carriers: 537
genotype depth: GenotypeDepth
  all individuals: 8176
  bin: 3.25e1
  variant carriers: 1422
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 1.75e1
  variant carriers: 411
genotype depth: GenotypeDepth
  all individuals: 5298
  bin: 4.25e1
  variant carriers: 2680
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 8.75e1
  variant carriers: 358
genotype depth: GenotypeDepth
  all individuals: 6611
  bin: 3.75e1
  variant carriers: 2171
genotype depth: GenotypeDepth
  all individuals: 3386
  bin: 5.25e1
  variant carriers: 2524
genotype depth: GenotypeDepth
  all individuals: 7164
  bin: 2.25e1
  variant carriers: 473
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 7.25e1
  variant carriers: 748
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 2.5e0
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 5.75e1
  variant carriers: 2132
genotype depth: GenotypeDepth
  all individuals: 4348
  bin: 4.75e1
  variant carriers: 2812
genotype depth: GenotypeDepth
  all individuals: 8489
  bin: 2.75e1
  variant carriers: 814
genotype depth: GenotypeDepth
  all individuals: 3242
  bin: 7.5e0
  variant carriers: 795
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 1.25e1
  variant carriers: 921
genotype depth: GenotypeDepth
  all individuals: 1334
  bin: 6.75e1
  variant carriers: 1017
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 9.75e1
  variant carriers: 1477
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 9.25e1
  variant carriers: 278
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 8.25e1
  variant carriers: 423
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 6.25e1
  variant carriers: 1531
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 3.75e1
  variant carriers: 81
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 8.75e1
  variant carriers: 130
genotype quality: GenotypeQuality
  all individuals: 3684
  bin: 6.75e1
  variant carriers: 79
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 3.25e1
  variant carriers: 87
num of homozygotes: 3102
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

11-82561340-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561340
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561340
    reference: chr 11
allele count: 1
allele frequency: 8.811504300014099e-6
allele num: 113488
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.278+26A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.278+26A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.656+26A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.278+26A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.470+26A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.278+26A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.278+26A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.278+26A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.278+26A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.593+26A>G
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5629
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11153
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7624
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10965
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1632
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2345
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2884
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 561
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

11-82561341-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561341
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561340
    reference: chr 11
allele count: 1
allele frequency: 8.812902088657796e-6
allele num: 113470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.593+24delG
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.278+24delG
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.278+24delG
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.278+24delG
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.470+24delG
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.278+24delG
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.278+24delG
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.278+24delG
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.278+24delG
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.656+24delG
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7640
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10968
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 646
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2174
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18019
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2822
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 242
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
reference allele: TC
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ

11-82561344-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561344
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561344
    reference: chr 11
allele count: 10
allele frequency: 8.797395970792646e-5
allele num: 113670
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.278+22A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.656+22A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.278+22A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.278+22A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.470+22A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.278+22A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.278+22A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.278+22A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.278+22A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.593+22A>G
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8058
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7748
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10983
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1630
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2171
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1374
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 474
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3661
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ

11-82561354-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561354
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561354
    reference: chr 11
allele count: 1
allele frequency: 8.736829229935872e-6
allele num: 114458
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.656+12T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.593+12T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.278+12T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.278+12T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.278+12T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.278+12T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.278+12T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.278+12T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.470+12T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.278+12T>C
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1622
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1369
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11284
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13470
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2346
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: A
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

11-82561357-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561357
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561357
    reference: chr 11
allele count: 2
allele frequency: 1.745261614716046e-5
allele num: 114596
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.278+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.278+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.278+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.278+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.656+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.278+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.278+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.593+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.278+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.470+9A>G
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8152
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11041
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5627
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13610
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 546
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

11-82561358-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561358
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561358
    reference: chr 11
allele count: 1
allele frequency: 8.723415391594117e-6
allele num: 114634
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.593+8C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.278+8C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.278+8C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.278+8C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.278+8C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.656+8C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.278+8C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.278+8C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.470+8C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.278+8C>T
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1591
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3062
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8187
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 5.75e1
  variant carriers: 0
hgvs: c.656+8C>T
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP

11-82561362-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561362
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561362
    reference: chr 11
allele count: 1
allele frequency: 8.68628609151871e-6
allele num: 115124
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.593+4A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.278+4A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.470+4A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.656+4A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.278+4A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.278+4A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.278+4A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.278+4A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.278+4A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.278+4A>G
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8066
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
hgvs: c.656+4A>G
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum

11-82561362-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561362
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561362
    reference: chr 11
allele count: 1
allele frequency: 8.68628609151871e-6
allele num: 115124
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.593+4A>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.278+4A>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.470+4A>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.278+4A>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.656+4A>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.278+4A>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.278+4A>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.278+4A>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.278+4A>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.278+4A>C
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11048
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8365
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11320
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18011
  bin: 9.75e1
  variant carriers: 1
hgvs: c.656+4A>C
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

http://identifiers.org/exac.variant/11-82561365-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561365
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561365
    reference: chr 11
allele count: 1
allele frequency: 8.674983083782986e-6
allele num: 115274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.278+1G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.278+1G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.278+1G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.278+1G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.470+1G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.278+1G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.593+1G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.656+1G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.278+1G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.278+1G>T
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8550
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11050
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5631
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 505
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2343
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2902
  bin: 7.25e1
  variant carriers: 0
hgvs: c.656+1G>T
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD

11-82561375-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561375
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561375
    reference: chr 11
allele count: 1
allele frequency: 8.575888033205839e-6
allele num: 116606
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.269T>C
  hgvsp: ENSP00000442077.1:p.Met90Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.269T>C
  hgvsp: ENSP00000435071.1:p.Met90Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.269T>C
  hgvsp: ENSP00000432506.1:p.Met90Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.269T>C
  hgvsp: ENSP00000431435.1:p.Met90Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.269T>C
  hgvsp: ENSP00000436141.1:p.Met90Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.647T>C
  hgvsp: ENSP00000377055.2:p.Met216Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.584T>C
  hgvsp: ENSP00000317362.3:p.Met195Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.269T>C
  hgvsp: ENSP00000432004.1:p.Met90Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.461T>C
  hgvsp: ENSP00000434771.1:p.Met154Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.269T>C
  hgvsp: ENSP00000431559.1:p.Met90Thr
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8065
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11437
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9314
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Met216Thr
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

11-82561376-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561376
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561376
    reference: chr 11
allele count: 1
allele frequency: 8.568833439015613e-6
allele num: 116702
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.268A>G
  hgvsp: ENSP00000435071.1:p.Met90Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.646A>G
  hgvsp: ENSP00000377055.2:p.Met216Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.583A>G
  hgvsp: ENSP00000317362.3:p.Met195Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.268A>G
  hgvsp: ENSP00000431435.1:p.Met90Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.268A>G
  hgvsp: ENSP00000436141.1:p.Met90Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.460A>G
  hgvsp: ENSP00000434771.1:p.Met154Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.268A>G
  hgvsp: ENSP00000432506.1:p.Met90Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.268A>G
  hgvsp: ENSP00000432004.1:p.Met90Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.268A>G
  hgvsp: ENSP00000442077.1:p.Met90Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.268A>G
  hgvsp: ENSP00000431559.1:p.Met90Val
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11445
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9392
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8066
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Met216Val
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/11-82561383-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561383
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561383
    reference: chr 11
allele count: 1
allele frequency: 8.511217785040683e-6
allele num: 117492
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.261T>G
  hgvsp: ENSP00000431435.1:p.Tyr87Ter
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.261T>G
  hgvsp: ENSP00000431559.1:p.Tyr87Ter
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.261T>G
  hgvsp: ENSP00000435071.1:p.Tyr87Ter
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.261T>G
  hgvsp: ENSP00000442077.1:p.Tyr87Ter
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.261T>G
  hgvsp: ENSP00000436141.1:p.Tyr87Ter
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.261T>G
  hgvsp: ENSP00000432506.1:p.Tyr87Ter
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.639T>G
  hgvsp: ENSP00000377055.2:p.Tyr213Ter
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.576T>G
  hgvsp: ENSP00000317362.3:p.Tyr192Ter
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.453T>G
  hgvsp: ENSP00000434771.1:p.Tyr151Ter
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.261T>G
  hgvsp: ENSP00000432004.1:p.Tyr87Ter
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11061
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8067
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2168
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Tyr213Ter
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD

11-82561386-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561386
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561386
    reference: chr 11
allele count: 1
allele frequency: 8.49314603115286e-6
allele num: 117742
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.258A>G
  hgvsp: ENST00000531801.1:c.258A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.258A>G
  hgvsp: ENST00000528082.1:c.258A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.636A>G
  hgvsp: ENST00000393399.2:c.636A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.258A>G
  hgvsp: ENST00000535099.1:c.258A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.258A>G
  hgvsp: ENST00000534396.1:c.258A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.258A>G
  hgvsp: ENST00000527444.1:c.258A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.573A>G
  hgvsp: ENST00000313010.3:c.573A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.258A>G
  hgvsp: ENST00000531128.1:c.258A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.258A>G
  hgvsp: ENST00000534631.1:c.258A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.450A>G
  hgvsp: ENST00000529671.1:c.450A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11067
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8067
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2915
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Lys212Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

11-82561403-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561403
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561403
    reference: chr 11
allele count: 9
allele frequency: 7.499500033331111e-5
allele num: 120008
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.619G>A
  hgvsp: ENSP00000377055.2:p.Ala207Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.241G>A
  hgvsp: ENSP00000431559.1:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.241G>A
  hgvsp: ENSP00000432506.1:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.556G>A
  hgvsp: ENSP00000317362.3:p.Ala186Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.241G>A
  hgvsp: ENSP00000432004.1:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.241G>A
  hgvsp: ENSP00000435071.1:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.241G>A
  hgvsp: ENSP00000431435.1:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.241G>A
  hgvsp: ENSP00000436141.1:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.241G>A
  hgvsp: ENSP00000442077.1:p.Ala81Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.433G>A
  hgvsp: ENSP00000434771.1:p.Ala145Thr
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11171
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8075
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11458
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 965
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala207Thr
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ

11-82561404-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561404
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561404
    reference: chr 11
allele count: 6
allele frequency: 4.992012779552715e-5
allele num: 120192
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.240C>T
  hgvsp: ENST00000535099.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.618C>T
  hgvsp: ENST00000393399.2:c.618C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.432C>T
  hgvsp: ENST00000529671.1:c.432C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.240C>T
  hgvsp: ENST00000534396.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.240C>T
  hgvsp: ENST00000527444.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.240C>T
  hgvsp: ENST00000528082.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.240C>T
  hgvsp: ENST00000531128.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.240C>T
  hgvsp: ENST00000534631.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.240C>T
  hgvsp: ENST00000531801.1:c.240C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.555C>T
  hgvsp: ENST00000313010.3:c.555C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 12108
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11583
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11134
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3661
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala206Ala
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum

11-82561414-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561414
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561414
    reference: chr 11
allele count: 1
allele frequency: 8.281573498964803e-6
allele num: 120750
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.608G>A
  hgvsp: ENSP00000377055.2:p.Gly203Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.230G>A
  hgvsp: ENSP00000435071.1:p.Gly77Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.230G>A
  hgvsp: ENSP00000431435.1:p.Gly77Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.230G>A
  hgvsp: ENSP00000436141.1:p.Gly77Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.230G>A
  hgvsp: ENSP00000432506.1:p.Gly77Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.230G>A
  hgvsp: ENSP00000442077.1:p.Gly77Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.230G>A
  hgvsp: ENSP00000432004.1:p.Gly77Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.545G>A
  hgvsp: ENSP00000317362.3:p.Gly182Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.230G>A
  hgvsp: ENSP00000431559.1:p.Gly77Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.422G>A
  hgvsp: ENSP00000434771.1:p.Gly141Asp
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5638
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12367
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8076
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly203Asp
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-82561419-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561419
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561419
    reference: chr 11
allele count: 1
allele frequency: 8.270751315049459e-6
allele num: 120908
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.603T>C
  hgvsp: ENST00000393399.2:c.603T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.225T>C
  hgvsp: ENST00000534396.1:c.225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.225T>C
  hgvsp: ENST00000531801.1:c.225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.225T>C
  hgvsp: ENST00000528082.1:c.225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.417T>C
  hgvsp: ENST00000529671.1:c.417T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.225T>C
  hgvsp: ENST00000535099.1:c.225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.225T>C
  hgvsp: ENST00000531128.1:c.225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.225T>C
  hgvsp: ENST00000527444.1:c.225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.225T>C
  hgvsp: ENST00000534631.1:c.225T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.540T>C
  hgvsp: ENST00000313010.3:c.540T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12443
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11796
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4743
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Tyr201Tyr
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/11-82561426-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561426
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561426
    reference: chr 11
allele count: 1
allele frequency: 8.262277744728666e-6
allele num: 121032
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.596G>T
  hgvsp: ENSP00000377055.2:p.Gly199Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.218G>T
  hgvsp: ENSP00000435071.1:p.Gly73Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.218G>T
  hgvsp: ENSP00000436141.1:p.Gly73Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.218G>T
  hgvsp: ENSP00000442077.1:p.Gly73Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.218G>T
  hgvsp: ENSP00000432004.1:p.Gly73Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.218G>T
  hgvsp: ENSP00000432506.1:p.Gly73Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.218G>T
  hgvsp: ENSP00000431435.1:p.Gly73Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.410G>T
  hgvsp: ENSP00000434771.1:p.Gly137Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.533G>T
  hgvsp: ENSP00000317362.3:p.Gly178Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.218G>T
  hgvsp: ENSP00000431559.1:p.Gly73Val
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4401
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gly199Val
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum

11-82561426-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561426
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561426
    reference: chr 11
allele count: 1
allele frequency: 8.262277744728666e-6
allele num: 121032
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.218G>A
  hgvsp: ENSP00000431435.1:p.Gly73Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.218G>A
  hgvsp: ENSP00000431559.1:p.Gly73Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.218G>A
  hgvsp: ENSP00000435071.1:p.Gly73Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.218G>A
  hgvsp: ENSP00000432004.1:p.Gly73Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.218G>A
  hgvsp: ENSP00000432506.1:p.Gly73Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.410G>A
  hgvsp: ENSP00000434771.1:p.Gly137Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.596G>A
  hgvsp: ENSP00000377055.2:p.Gly199Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.533G>A
  hgvsp: ENSP00000317362.3:p.Gly178Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.218G>A
  hgvsp: ENSP00000442077.1:p.Gly73Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.218G>A
  hgvsp: ENSP00000436141.1:p.Gly73Asp
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11185
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11841
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 209
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly199Asp
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

11-82561428-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561428
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561428
    reference: chr 11
allele count: 1
allele frequency: 8.258729477057249e-6
allele num: 121084
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.216A>C
  hgvsp: ENST00000531128.1:c.216A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.594A>C
  hgvsp: ENST00000393399.2:c.594A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.408A>C
  hgvsp: ENST00000529671.1:c.408A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.216A>C
  hgvsp: ENST00000534631.1:c.216A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.216A>C
  hgvsp: ENST00000534396.1:c.216A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.216A>C
  hgvsp: ENST00000535099.1:c.216A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.216A>C
  hgvsp: ENST00000527444.1:c.216A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.531A>C
  hgvsp: ENST00000313010.3:c.531A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.216A>C
  hgvsp: ENST00000531801.1:c.216A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.216A>C
  hgvsp: ENST00000528082.1:c.216A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11177
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18001
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gly198Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

11-82561429-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561429
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561429
    reference: chr 11
allele count: 1
allele frequency: 8.256683785524381e-6
allele num: 121114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.407G>A
  hgvsp: ENSP00000434771.1:p.Gly136Glu
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.215G>A
  hgvsp: ENSP00000432506.1:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.593G>A
  hgvsp: ENSP00000377055.2:p.Gly198Glu
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.215G>A
  hgvsp: ENSP00000431559.1:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.215G>A
  hgvsp: ENSP00000442077.1:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.215G>A
  hgvsp: ENSP00000431435.1:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.215G>A
  hgvsp: ENSP00000432004.1:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.530G>A
  hgvsp: ENSP00000317362.3:p.Gly177Glu
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.215G>A
  hgvsp: ENSP00000436141.1:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.215G>A
  hgvsp: ENSP00000435071.1:p.Gly72Glu
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11180
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11891
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly198Glu
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
reference allele: C
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

11-82561432-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561432
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561432
    reference: chr 11
allele count: 2
allele frequency: 1.651145895251304e-5
allele num: 121128
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.212T>C
  hgvsp: ENSP00000432004.1:p.Ile71Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.527T>C
  hgvsp: ENSP00000317362.3:p.Ile176Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.212T>C
  hgvsp: ENSP00000432506.1:p.Ile71Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.212T>C
  hgvsp: ENSP00000431435.1:p.Ile71Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.212T>C
  hgvsp: ENSP00000442077.1:p.Ile71Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.404T>C
  hgvsp: ENSP00000434771.1:p.Ile135Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.212T>C
  hgvsp: ENSP00000431559.1:p.Ile71Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.590T>C
  hgvsp: ENSP00000377055.2:p.Ile197Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.212T>C
  hgvsp: ENSP00000436141.1:p.Ile71Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.212T>C
  hgvsp: ENSP00000435071.1:p.Ile71Thr
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11179
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11905
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12527
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile197Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: A
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD

11-82561433-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561433
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561433
    reference: chr 11
allele count: 1
allele frequency: 8.255047961828658e-6
allele num: 121138
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.526A>G
  hgvsp: ENSP00000317362.3:p.Ile176Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.211A>G
  hgvsp: ENSP00000432004.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.589A>G
  hgvsp: ENSP00000377055.2:p.Ile197Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.211A>G
  hgvsp: ENSP00000436141.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.211A>G
  hgvsp: ENSP00000435071.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.211A>G
  hgvsp: ENSP00000431435.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.211A>G
  hgvsp: ENSP00000442077.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.211A>G
  hgvsp: ENSP00000432506.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.211A>G
  hgvsp: ENSP00000431559.1:p.Ile71Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.403A>G
  hgvsp: ENSP00000434771.1:p.Ile135Val
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12530
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11904
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11183
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 154
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ile197Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: QD

11-82561435-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561435
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561435
    reference: chr 11
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.587C>G
  hgvsp: ENSP00000377055.2:p.Ala196Gly
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.209C>G
  hgvsp: ENSP00000432004.1:p.Ala70Gly
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.209C>G
  hgvsp: ENSP00000431559.1:p.Ala70Gly
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.209C>G
  hgvsp: ENSP00000435071.1:p.Ala70Gly
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.401C>G
  hgvsp: ENSP00000434771.1:p.Ala134Gly
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.209C>G
  hgvsp: ENSP00000436141.1:p.Ala70Gly
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.209C>G
  hgvsp: ENSP00000432506.1:p.Ala70Gly
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.524C>G
  hgvsp: ENSP00000317362.3:p.Ala175Gly
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.209C>G
  hgvsp: ENSP00000431435.1:p.Ala70Gly
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.209C>G
  hgvsp: ENSP00000442077.1:p.Ala70Gly
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1368
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11184
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala196Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

11-82561439-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561439
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561439
    reference: chr 11
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.205A>T
  hgvsp: ENSP00000431435.1:p.Ile69Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.205A>T
  hgvsp: ENSP00000432004.1:p.Ile69Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.520A>T
  hgvsp: ENSP00000317362.3:p.Ile174Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.205A>T
  hgvsp: ENSP00000431559.1:p.Ile69Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.205A>T
  hgvsp: ENSP00000436141.1:p.Ile69Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.205A>T
  hgvsp: ENSP00000432506.1:p.Ile69Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.583A>T
  hgvsp: ENSP00000377055.2:p.Ile195Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.205A>T
  hgvsp: ENSP00000442077.1:p.Ile69Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.205A>T
  hgvsp: ENSP00000435071.1:p.Ile69Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.397A>T
  hgvsp: ENSP00000434771.1:p.Ile133Phe
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11186
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4736
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ile195Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD

11-82561444-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561444
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561444
    reference: chr 11
allele count: 1
allele frequency: 8.250280509537325e-6
allele num: 121208
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.200C>G
  hgvsp: ENSP00000436141.1:p.Pro67Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.200C>G
  hgvsp: ENSP00000431559.1:p.Pro67Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.200C>G
  hgvsp: ENSP00000432506.1:p.Pro67Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.515C>G
  hgvsp: ENSP00000317362.3:p.Pro172Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.578C>G
  hgvsp: ENSP00000377055.2:p.Pro193Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.200C>G
  hgvsp: ENSP00000432004.1:p.Pro67Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.200C>G
  hgvsp: ENSP00000431435.1:p.Pro67Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.200C>G
  hgvsp: ENSP00000435071.1:p.Pro67Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.200C>G
  hgvsp: ENSP00000442077.1:p.Pro67Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.392C>G
  hgvsp: ENSP00000434771.1:p.Pro131Arg
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11187
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5633
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro193Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-82561456-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561456
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561456
    reference: chr 11
allele count: 39
allele frequency: 3.216919346058036e-4
allele num: 121234
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.188C>T
  hgvsp: ENSP00000432506.1:p.Ala63Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.188C>T
  hgvsp: ENSP00000436141.1:p.Ala63Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.188C>T
  hgvsp: ENSP00000431435.1:p.Ala63Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.188C>T
  hgvsp: ENSP00000442077.1:p.Ala63Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.188C>T
  hgvsp: ENSP00000431559.1:p.Ala63Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.566C>T
  hgvsp: ENSP00000377055.2:p.Ala189Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.188C>T
  hgvsp: ENSP00000435071.1:p.Ala63Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.188C>T
  hgvsp: ENSP00000432004.1:p.Ala63Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.341C>T
  hgvsp: ENSP00000437169.1:p.Ala114Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.503C>T
  hgvsp: ENSP00000317362.3:p.Ala168Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.380C>T
  hgvsp: ENSP00000434771.1:p.Ala127Val
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11185
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8071
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11916
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12577
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1367
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala189Val
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: VQSLOD

11-82561462-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561462
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561462
    reference: chr 11
allele count: 1
allele frequency: 8.249191579225235e-6
allele num: 121224
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.560C>A
  hgvsp: ENSP00000377055.2:p.Pro187Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.182C>A
  hgvsp: ENSP00000435071.1:p.Pro61Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.182C>A
  hgvsp: ENSP00000432004.1:p.Pro61Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.182C>A
  hgvsp: ENSP00000432506.1:p.Pro61Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.497C>A
  hgvsp: ENSP00000317362.3:p.Pro166Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.374C>A
  hgvsp: ENSP00000434771.1:p.Pro125Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.182C>A
  hgvsp: ENSP00000431559.1:p.Pro61Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.182C>A
  hgvsp: ENSP00000431435.1:p.Pro61Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.182C>A
  hgvsp: ENSP00000436141.1:p.Pro61Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.182C>A
  hgvsp: ENSP00000442077.1:p.Pro61Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.335C>A
  hgvsp: ENSP00000437169.1:p.Pro112Gln
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11914
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11191
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro187Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: QD

11-82561480-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561480
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561480
    reference: chr 11
allele count: 1
allele frequency: 8.253957772752034e-6
allele num: 121154
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.542A>G
  hgvsp: ENSP00000377055.2:p.His181Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.164A>G
  hgvsp: ENSP00000431559.1:p.His55Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.164A>G
  hgvsp: ENSP00000442077.1:p.His55Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.317A>G
  hgvsp: ENSP00000437169.1:p.His106Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.164A>G
  hgvsp: ENSP00000431435.1:p.His55Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.164A>G
  hgvsp: ENSP00000432506.1:p.His55Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.164A>G
  hgvsp: ENSP00000435071.1:p.His55Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.479A>G
  hgvsp: ENSP00000317362.3:p.His160Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.164A>G
  hgvsp: ENSP00000432004.1:p.His55Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.356A>G
  hgvsp: ENSP00000434771.1:p.His119Arg
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.164A>G
  hgvsp: ENSP00000436141.1:p.His55Arg
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12597
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His181Arg
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum

11-82561487-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561487
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561487
    reference: chr 11
allele count: 1
allele frequency: 8.259820927082301e-6
allele num: 121068
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.157A>G
  hgvsp: ENSP00000432506.1:p.Ile53Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.157A>G
  hgvsp: ENSP00000435071.1:p.Ile53Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.157A>G
  hgvsp: ENSP00000432004.1:p.Ile53Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.157A>G
  hgvsp: ENSP00000442077.1:p.Ile53Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.535A>G
  hgvsp: ENSP00000377055.2:p.Ile179Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.157A>G
  hgvsp: ENSP00000431559.1:p.Ile53Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.310A>G
  hgvsp: ENSP00000437169.1:p.Ile104Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.349A>G
  hgvsp: ENSP00000434771.1:p.Ile117Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.472A>G
  hgvsp: ENSP00000317362.3:p.Ile158Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.157A>G
  hgvsp: ENSP00000431435.1:p.Ile53Val
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.157A>G
  hgvsp: ENSP00000436141.1:p.Ile53Val
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11181
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5632
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12600
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11698
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile179Val
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ

11-82561499-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561499
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561499
    reference: chr 11
allele count: 1
allele frequency: 8.284455048546906e-6
allele num: 120708
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.523T>A
  hgvsp: ENSP00000377055.2:p.Phe175Ile
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.298T>A
  hgvsp: ENSP00000437169.1:p.Phe100Ile
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.145T>A
  hgvsp: ENSP00000435071.1:p.Phe49Ile
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.460T>A
  hgvsp: ENSP00000317362.3:p.Phe154Ile
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.337T>A
  hgvsp: ENSP00000434771.1:p.Phe113Ile
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.145T>A
  hgvsp: ENSP00000432506.1:p.Phe49Ile
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.145T>A
  hgvsp: ENSP00000431435.1:p.Phe49Ile
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.145T>A
  hgvsp: ENSP00000442077.1:p.Phe49Ile
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.145T>A
  hgvsp: ENSP00000431559.1:p.Phe49Ile
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.145T>A
  hgvsp: ENSP00000436141.1:p.Phe49Ile
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.145T>A
  hgvsp: ENSP00000432004.1:p.Phe49Ile
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11311
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11178
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe175Ile
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

11-82561502-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561502
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561502
    reference: chr 11
allele count: 1
allele frequency: 8.293799555452344e-6
allele num: 120572
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.295G>C
  hgvsp: ENSP00000437169.1:p.Asp99His
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.142G>C
  hgvsp: ENSP00000435071.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.142G>C
  hgvsp: ENSP00000431559.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.142G>C
  hgvsp: ENSP00000431435.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.334G>C
  hgvsp: ENSP00000434771.1:p.Asp112His
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.142G>C
  hgvsp: ENSP00000432506.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.520G>C
  hgvsp: ENSP00000377055.2:p.Asp174His
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.457G>C
  hgvsp: ENSP00000317362.3:p.Asp153His
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.142G>C
  hgvsp: ENSP00000432004.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.142G>C
  hgvsp: ENSP00000436141.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.142G>C
  hgvsp: ENSP00000442077.1:p.Asp48His
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11208
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12492
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp174His
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD

11-82561506-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561506
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561506
    reference: chr 11
allele count: 1
allele frequency: 8.31255195344971e-6
allele num: 120300
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.138G>A
  hgvsp: ENST00000528082.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.138G>A
  hgvsp: ENST00000527444.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.138G>A
  hgvsp: ENST00000535099.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.330G>A
  hgvsp: ENST00000529671.1:c.330G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.138G>A
  hgvsp: ENST00000534396.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.138G>A
  hgvsp: ENST00000531128.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.138G>A
  hgvsp: ENST00000534631.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.138G>A
  hgvsp: ENST00000531801.1:c.138G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.291G>A
  hgvsp: ENST00000532809.1:c.291G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.516G>A
  hgvsp: ENST00000393399.2:c.516G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.453G>A
  hgvsp: ENST00000313010.3:c.453G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12436
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10960
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 884
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11172
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu172Leu
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum

11-82561517-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561517
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561517
    reference: chr 11
allele count: 1
allele frequency: 8.367500627562547e-6
allele num: 119510
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.127G>C
  hgvsp: ENSP00000432506.1:p.Glu43Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.505G>C
  hgvsp: ENSP00000377055.2:p.Glu169Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.127G>C
  hgvsp: ENSP00000431496.1:p.Glu43Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.319G>C
  hgvsp: ENSP00000434771.1:p.Glu107Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.127G>C
  hgvsp: ENSP00000432004.1:p.Glu43Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.127G>C
  hgvsp: ENSP00000442077.1:p.Glu43Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.127G>C
  hgvsp: ENSP00000431559.1:p.Glu43Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.280G>C
  hgvsp: ENSP00000437169.1:p.Glu94Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.442G>C
  hgvsp: ENSP00000317362.3:p.Glu148Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.127G>C
  hgvsp: ENSP00000431435.1:p.Glu43Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.127G>C
  hgvsp: ENSP00000435071.1:p.Glu43Gln
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.127G>C
  hgvsp: ENSP00000436141.1:p.Glu43Gln
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8071
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10303
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu169Gln
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum

11-82561518-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561518
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561518
    reference: chr 11
allele count: 1
allele frequency: 8.372264362619514e-6
allele num: 119442
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.126A>G
  hgvsp: ENST00000534631.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.126A>G
  hgvsp: ENST00000533126.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.126A>G
  hgvsp: ENST00000531128.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.126A>G
  hgvsp: ENST00000531801.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.279A>G
  hgvsp: ENST00000532809.1:c.279A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.126A>G
  hgvsp: ENST00000534396.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.318A>G
  hgvsp: ENST00000529671.1:c.318A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.126A>G
  hgvsp: ENST00000527444.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.504A>G
  hgvsp: ENST00000393399.2:c.504A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.441A>G
  hgvsp: ENST00000313010.3:c.441A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.126A>G
  hgvsp: ENST00000528082.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.126A>G
  hgvsp: ENST00000535099.1:c.126A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8070
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10248
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser168Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum

11-82561536-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561536
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561536
    reference: chr 11
allele count: 4
allele frequency: 3.39662375598655e-5
allele num: 117764
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.300C>T
  hgvsp: ENST00000529671.1:c.300C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.108C>T
  hgvsp: ENST00000534631.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.423C>T
  hgvsp: ENST00000313010.3:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.108C>T
  hgvsp: ENST00000528082.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.108C>T
  hgvsp: ENST00000531801.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.261C>T
  hgvsp: ENST00000532809.1:c.261C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.108C>T
  hgvsp: ENST00000531128.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.108C>T
  hgvsp: ENST00000534396.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.108C>T
  hgvsp: ENST00000533126.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.486C>T
  hgvsp: ENST00000393399.2:c.486C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.108C>T
  hgvsp: ENST00000535099.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.108C>T
  hgvsp: ENST00000527444.1:c.108C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5630
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2108
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8063
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11636
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.His162His
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

11-82561538-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561538
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561538
    reference: chr 11
allele count: 1
allele frequency: 8.510493438409559e-6
allele num: 117502
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.106C>A
  hgvsp: ENSP00000442077.1:p.His36Asn
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.259C>A
  hgvsp: ENSP00000437169.1:p.His87Asn
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.106C>A
  hgvsp: ENSP00000432004.1:p.His36Asn
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.106C>A
  hgvsp: ENSP00000431559.1:p.His36Asn
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.484C>A
  hgvsp: ENSP00000377055.2:p.His162Asn
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.106C>A
  hgvsp: ENSP00000431435.1:p.His36Asn
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.106C>A
  hgvsp: ENSP00000432506.1:p.His36Asn
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.421C>A
  hgvsp: ENSP00000317362.3:p.His141Asn
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.106C>A
  hgvsp: ENSP00000436141.1:p.His36Asn
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.106C>A
  hgvsp: ENSP00000431496.1:p.His36Asn
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.106C>A
  hgvsp: ENSP00000435071.1:p.His36Asn
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.298C>A
  hgvsp: ENSP00000434771.1:p.His100Asn
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5629
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3536
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His162Asn
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP

11-82561544-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561544
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561544
    reference: chr 11
allele count: 1
allele frequency: 8.57368222504201e-6
allele num: 116636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.253T>A
  hgvsp: ENSP00000437169.1:p.Ser85Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.100T>A
  hgvsp: ENSP00000442077.1:p.Ser34Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.100T>A
  hgvsp: ENSP00000436141.1:p.Ser34Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.100T>A
  hgvsp: ENSP00000431559.1:p.Ser34Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.100T>A
  hgvsp: ENSP00000431496.1:p.Ser34Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.100T>A
  hgvsp: ENSP00000432506.1:p.Ser34Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.478T>A
  hgvsp: ENSP00000377055.2:p.Ser160Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.100T>A
  hgvsp: ENSP00000435071.1:p.Ser34Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.100T>A
  hgvsp: ENSP00000432004.1:p.Ser34Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.415T>A
  hgvsp: ENSP00000317362.3:p.Ser139Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.292T>A
  hgvsp: ENSP00000434771.1:p.Ser98Thr
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.100T>A
  hgvsp: ENSP00000431435.1:p.Ser34Thr
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10934
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2733
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser160Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD

11-82561559-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561559
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561559
    reference: chr 11
allele count: 1
allele frequency: 8.672876446202148e-6
allele num: 115302
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.475-12A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.97-12A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.97-12A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.97-12A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.97-12A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.97-12A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.250-12A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.97-12A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.412-12A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.97-12A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.97-12A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.289-12A>G
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10854
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5624
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1365
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD

11-82561569-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561569
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561569
    reference: chr 11
allele count: 1
allele frequency: 8.785493393308968e-6
allele num: 113824
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.289-22G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.97-22G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.412-22G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.97-22G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.475-22G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.97-22G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.97-22G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.250-22G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.97-22G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.97-22G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.97-22G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.97-22G>A
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7097
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2778
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 848
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5627
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10695
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD

11-82561571-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561571
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561571
    reference: chr 11
allele count: 3
allele frequency: 2.642752691203157e-5
allele num: 113518
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.475-24G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.97-24G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.412-24G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.97-24G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.97-24G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.97-24G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.97-24G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.97-24G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.250-24G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.289-24G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.97-24G>A
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.97-24G>A
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10648
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2864
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7023
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 541
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5628
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

11-82561572-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561572
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561572
    reference: chr 11
allele count: 38
allele frequency: 3.354282889626439e-4
allele num: 113288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.97-25C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.412-25C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.97-25C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.97-25C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.97-25C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.97-25C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.97-25C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.97-25C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.97-25C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.475-25C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.289-25C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.250-25C>T
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 964
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10728
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2920
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10571
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1370
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3085
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 887
  bin: 6.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5622
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8012
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 1.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

11-82561584-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561584
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561584
    reference: chr 11
allele count: 3
allele frequency: 2.690341673392521e-5
allele num: 111510
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.250-37C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.97-37C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.97-37C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.475-37C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.97-37C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.97-37C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.97-37C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.97-37C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.97-37C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.97-37C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.412-37C>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.289-37C>T
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3532
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2705
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7985
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1378
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10422
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3372
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

11-82561589-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561589
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561589
    reference: chr 11
allele count: 5
allele frequency: 4.500531062665394e-5
allele num: 111098
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.97-42A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.475-42A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.97-42A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.289-42A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.250-42A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.97-42A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.97-42A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.412-42A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.97-42A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.97-42A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.97-42A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.97-42A>G
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10230
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7932
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9723
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5605
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2500
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6247
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

11-82561595-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561595
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561595
    reference: chr 11
allele count: 2
allele frequency: 1.811430124082963e-5
allele num: 110410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.97-48G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.97-48G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.475-48G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.97-48G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.97-48G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.412-48G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.97-48G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.97-48G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.250-48G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.97-48G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.289-48G>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.97-48G>C
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2169
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2225
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9423
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7010
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: C
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff

11-82561596-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82561596
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82561596
    reference: chr 11
allele count: 3
allele frequency: 2.71684990309902e-5
allele num: 110422
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.250-49T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.289-49T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.97-49T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.97-49T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.97-49T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.97-49T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.97-49T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.412-49T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.97-49T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.97-49T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.475-49T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.97-49T>C
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5595
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2213
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9760
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3529
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9424
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 960
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3847
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

11-82564182-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564182
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564182
    reference: chr 11
allele count: 1
allele frequency: 1.069198528782824e-5
allele num: 93528
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.96+37T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.474+37T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.411+37T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.96+37T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.96+37T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.288+37T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.96+37T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.96+37T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.96+37T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.96+37T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.96+37T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.249+37T>C
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5213
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1298
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16849
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17262
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12523
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD

http://identifiers.org/exac.variant/11-82564186-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564186
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564186
    reference: chr 11
allele count: 1
allele frequency: 1.055052647127092e-5
allele num: 94782
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.96+33T>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.96+33T>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.96+33T>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.96+33T>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.96+33T>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.96+33T>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.96+33T>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.288+33T>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.411+33T>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.249+33T>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.474+33T>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.96+33T>G
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3363
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1375
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD

11-82564193-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564193
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564193
    reference: chr 11
allele count: 1
allele frequency: 9.980836793356755e-6
allele num: 100192
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.288+26T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.96+26T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.96+26T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.411+26T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.96+26T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.474+26T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.96+26T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.96+26T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.96+26T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.96+26T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.249+26T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.96+26T>C
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31098
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8044
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1611
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4442
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10121
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 740
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

http://identifiers.org/exac.variant/11-82564195-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564195
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564195
    reference: chr 11
allele count: 1
allele frequency: 9.799118079372857e-6
allele num: 102050
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.411+24G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.288+24G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.249+24G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.96+24G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.96+24G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.474+24G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.96+24G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.96+24G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.96+24G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.96+24G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.96+24G>T
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.96+24G>T
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 744
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33371
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4779
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9228
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD

11-82564200-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564200
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564200
    reference: chr 11
allele count: 1
allele frequency: 9.332885354836302e-6
allele num: 107148
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.96+19T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.96+19T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.288+19T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.96+19T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.96+19T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.96+19T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.96+19T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.474+19T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.96+19T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.411+19T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.96+19T>C
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.249+19T>C
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 770
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3802
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38369
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6892
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5346
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

11-82564202-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564202
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564202
    reference: chr 11
allele count: 1
allele frequency: 9.178522257916476e-6
allele num: 108950
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.96+17C>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.288+17C>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.96+17C>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.96+17C>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.249+17C>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.411+17C>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.96+17C>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.474+17C>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.96+17C>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.96+17C>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.96+17C>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.96+17C>G
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5666
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 765
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6022
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3089
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2039
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD
site quality: MQ

11-82564210-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564210
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564210
    reference: chr 11
allele count: 2
allele frequency: 1.73565911654951e-5
allele num: 115230
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.96+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.96+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.249+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.96+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.288+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.96+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.96+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.411+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.96+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.96+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.96+9A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.474+9A>G
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3007
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6646
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

11-82564214-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564214
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564214
    reference: chr 11
allele count: 1
allele frequency: 8.507886811073865e-6
allele num: 117538
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.96+5A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.474+5A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.249+5A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.411+5A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.288+5A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.96+5A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.96+5A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.96+5A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.96+5A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.96+5A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.96+5A>G
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.96+5A>G
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44865
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7015
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.474+5A>G
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

11-82564234-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564234
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564234
    reference: chr 11
allele count: 1
allele frequency: 8.278556881964336e-6
allele num: 120794
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.81T>C
  hgvsp: ENST00000534631.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.396T>C
  hgvsp: ENST00000313010.3:c.396T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.81T>C
  hgvsp: ENST00000533126.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.81T>C
  hgvsp: ENST00000531128.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.81T>C
  hgvsp: ENST00000534396.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.81T>C
  hgvsp: ENST00000535099.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.273T>C
  hgvsp: ENST00000529671.1:c.273T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.81T>C
  hgvsp: ENST00000531801.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.81T>C
  hgvsp: ENST00000528082.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.81T>C
  hgvsp: ENST00000527444.1:c.81T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.459T>C
  hgvsp: ENST00000393399.2:c.459T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.234T>C
  hgvsp: ENST00000532809.1:c.234T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 46035
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7873
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly153Gly
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
reference allele: A
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

11-82564244-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564244
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564244
    reference: chr 11
allele count: 1
allele frequency: 8.261049153242462e-6
allele num: 121050
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.71T>C
  hgvsp: ENSP00000432506.1:p.Leu24Pro
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.386T>C
  hgvsp: ENSP00000317362.3:p.Leu129Pro
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.71T>C
  hgvsp: ENSP00000431496.1:p.Leu24Pro
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.71T>C
  hgvsp: ENSP00000432004.1:p.Leu24Pro
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.449T>C
  hgvsp: ENSP00000377055.2:p.Leu150Pro
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.71T>C
  hgvsp: ENSP00000435071.1:p.Leu24Pro
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436095
  ensembl transcript: ENST00000534264
  gene symbol: PRCP
  hgvsc: ENST00000534264.1:c.71T>C
  hgvsp: ENSP00000436095.1:p.Leu24Pro
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.71T>C
  hgvsp: ENSP00000431435.1:p.Leu24Pro
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.71T>C
  hgvsp: ENSP00000431559.1:p.Leu24Pro
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.71T>C
  hgvsp: ENSP00000436141.1:p.Leu24Pro
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.224T>C
  hgvsp: ENSP00000437169.1:p.Leu75Pro
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.263T>C
  hgvsp: ENSP00000434771.1:p.Leu88Pro
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.71T>C
  hgvsp: ENSP00000442077.1:p.Leu24Pro
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2845
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu150Pro
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: DP

11-82564245-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564245
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564245
    reference: chr 11
allele count: 2
allele frequency: 1.65218253312626e-5
allele num: 121052
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.70C>T
  hgvsp: ENSP00000442077.1:p.Leu24Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.70C>T
  hgvsp: ENSP00000432506.1:p.Leu24Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.70C>T
  hgvsp: ENSP00000432004.1:p.Leu24Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.448C>T
  hgvsp: ENSP00000377055.2:p.Leu150Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.70C>T
  hgvsp: ENSP00000431496.1:p.Leu24Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.262C>T
  hgvsp: ENSP00000434771.1:p.Leu88Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.70C>T
  hgvsp: ENSP00000431559.1:p.Leu24Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.70C>T
  hgvsp: ENSP00000435071.1:p.Leu24Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.70C>T
  hgvsp: ENSP00000436141.1:p.Leu24Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436095
  ensembl transcript: ENST00000534264
  gene symbol: PRCP
  hgvsc: ENST00000534264.1:c.70C>T
  hgvsp: ENSP00000436095.1:p.Leu24Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.385C>T
  hgvsp: ENSP00000317362.3:p.Leu129Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.70C>T
  hgvsp: ENSP00000431435.1:p.Leu24Phe
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.223C>T
  hgvsp: ENSP00000437169.1:p.Leu75Phe
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45920
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu150Phe
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

11-82564246-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564246
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564246
    reference: chr 11
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.69T>C
  hgvsp: ENST00000527444.1:c.69T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.69T>C
  hgvsp: ENST00000533126.1:c.69T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.222T>C
  hgvsp: ENST00000532809.1:c.222T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.69T>C
  hgvsp: ENST00000528082.1:c.69T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.69T>C
  hgvsp: ENST00000534631.1:c.69T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.384T>C
  hgvsp: ENST00000313010.3:c.384T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436095
  ensembl transcript: ENST00000534264
  gene symbol: PRCP
  hgvsc: ENST00000534264.1:c.69T>C
  hgvsp: ENST00000534264.1:c.69T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.69T>C
  hgvsp: ENST00000534396.1:c.69T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.69T>C
  hgvsp: ENST00000531128.1:c.69T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.69T>C
  hgvsp: ENST00000535099.1:c.69T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.261T>C
  hgvsp: ENST00000529671.1:c.261T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.447T>C
  hgvsp: ENST00000393399.2:c.447T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.69T>C
  hgvsp: ENST00000531801.1:c.69T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45910
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser149Ser
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

11-82564249-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564249
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564249
    reference: chr 11
allele count: 1
allele frequency: 8.256002113536541e-6
allele num: 121124
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.66G>C
  hgvsp: ENSP00000442077.1:p.Glu22Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.258G>C
  hgvsp: ENSP00000434771.1:p.Glu86Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.66G>C
  hgvsp: ENSP00000431496.1:p.Glu22Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.66G>C
  hgvsp: ENSP00000431435.1:p.Glu22Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.381G>C
  hgvsp: ENSP00000317362.3:p.Glu127Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.66G>C
  hgvsp: ENSP00000431559.1:p.Glu22Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.444G>C
  hgvsp: ENSP00000377055.2:p.Glu148Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.66G>C
  hgvsp: ENSP00000432506.1:p.Glu22Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.66G>C
  hgvsp: ENSP00000436141.1:p.Glu22Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.66G>C
  hgvsp: ENSP00000432004.1:p.Glu22Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436095
  ensembl transcript: ENST00000534264
  gene symbol: PRCP
  hgvsc: ENST00000534264.1:c.66G>C
  hgvsp: ENSP00000436095.1:p.Glu22Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.66G>C
  hgvsp: ENSP00000435071.1:p.Glu22Asp
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.219G>C
  hgvsp: ENSP00000437169.1:p.Glu73Asp
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45894
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8110
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu148Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum

11-82564255-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564255
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564255
    reference: chr 11
allele count: 7
allele frequency: 5.776816808886395e-5
allele num: 121174
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.60T>C
  hgvsp: ENST00000534396.1:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.60T>C
  hgvsp: ENST00000527444.1:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.375T>C
  hgvsp: ENST00000313010.3:c.375T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.60T>C
  hgvsp: ENST00000531128.1:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.60T>C
  hgvsp: ENST00000533126.1:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.60T>C
  hgvsp: ENST00000528082.1:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.438T>C
  hgvsp: ENST00000393399.2:c.438T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.213T>C
  hgvsp: ENST00000532809.1:c.213T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.252T>C
  hgvsp: ENST00000529671.1:c.252T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436095
  ensembl transcript: ENST00000534264
  gene symbol: PRCP
  hgvsc: ENST00000534264.1:c.60T>C
  hgvsp: ENST00000534264.1:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.60T>C
  hgvsp: ENST00000535099.1:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.60T>C
  hgvsp: ENST00000534631.1:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.60T>C
  hgvsp: ENST00000531801.1:c.60T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 617
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr146Tyr
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

11-82564256-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564256
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564256
    reference: chr 11
allele count: 1
allele frequency: 8.251914444151043e-6
allele num: 121184
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.251A>G
  hgvsp: ENSP00000434771.1:p.Tyr84Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436095
  ensembl transcript: ENST00000534264
  gene symbol: PRCP
  hgvsc: ENST00000534264.1:c.59A>G
  hgvsp: ENSP00000436095.1:p.Tyr20Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.59A>G
  hgvsp: ENSP00000431559.1:p.Tyr20Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.59A>G
  hgvsp: ENSP00000432004.1:p.Tyr20Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.59A>G
  hgvsp: ENSP00000435071.1:p.Tyr20Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.59A>G
  hgvsp: ENSP00000442077.1:p.Tyr20Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.59A>G
  hgvsp: ENSP00000436141.1:p.Tyr20Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.59A>G
  hgvsp: ENSP00000431496.1:p.Tyr20Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.59A>G
  hgvsp: ENSP00000431435.1:p.Tyr20Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.59A>G
  hgvsp: ENSP00000432506.1:p.Tyr20Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.374A>G
  hgvsp: ENSP00000317362.3:p.Tyr125Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.437A>G
  hgvsp: ENSP00000377055.2:p.Tyr146Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.212A>G
  hgvsp: ENSP00000437169.1:p.Tyr71Cys
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45873
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8162
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr146Cys
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum

11-82564258-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564258
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564258
    reference: chr 11
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.57C>T
  hgvsp: ENST00000535099.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.210C>T
  hgvsp: ENST00000532809.1:c.210C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.249C>T
  hgvsp: ENST00000529671.1:c.249C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.435C>T
  hgvsp: ENST00000393399.2:c.435C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.372C>T
  hgvsp: ENST00000313010.3:c.372C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.57C>T
  hgvsp: ENST00000531128.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436095
  ensembl transcript: ENST00000534264
  gene symbol: PRCP
  hgvsc: ENST00000534264.1:c.57C>T
  hgvsp: ENST00000534264.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.57C>T
  hgvsp: ENST00000533126.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.57C>T
  hgvsp: ENST00000527444.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.57C>T
  hgvsp: ENST00000531801.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.57C>T
  hgvsp: ENST00000534396.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.57C>T
  hgvsp: ENST00000534631.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.57C>T
  hgvsp: ENST00000528082.1:c.57C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8173
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr145Tyr
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: QD

11-82564259-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 82564259
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 82564259
    reference: chr 11
allele count: 1
allele frequency: 8.250416646040625e-6
allele num: 121206
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000434771
  ensembl transcript: ENST00000529671
  gene symbol: PRCP
  hgvsc: ENST00000529671.1:c.248A>G
  hgvsp: ENSP00000434771.1:p.Tyr83Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432004
  ensembl transcript: ENST00000531801
  gene symbol: PRCP
  hgvsc: ENST00000531801.1:c.56A>G
  hgvsp: ENSP00000432004.1:p.Tyr19Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436141
  ensembl transcript: ENST00000527444
  gene symbol: PRCP
  hgvsc: ENST00000527444.1:c.56A>G
  hgvsp: ENSP00000436141.1:p.Tyr19Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000442077
  ensembl transcript: ENST00000535099
  gene symbol: PRCP
  hgvsc: ENST00000535099.1:c.56A>G
  hgvsp: ENSP00000442077.1:p.Tyr19Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000377055
  ensembl transcript: ENST00000393399
  gene symbol: PRCP
  hgvsc: ENST00000393399.2:c.434A>G
  hgvsp: ENSP00000377055.2:p.Tyr145Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431496
  ensembl transcript: ENST00000533126
  gene symbol: PRCP
  hgvsc: ENST00000533126.1:c.56A>G
  hgvsp: ENSP00000431496.1:p.Tyr19Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000432506
  ensembl transcript: ENST00000534396
  gene symbol: PRCP
  hgvsc: ENST00000534396.1:c.56A>G
  hgvsp: ENSP00000432506.1:p.Tyr19Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000437169
  ensembl transcript: ENST00000532809
  gene symbol: PRCP
  hgvsc: ENST00000532809.1:c.209A>G
  hgvsp: ENSP00000437169.1:p.Tyr70Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000435071
  ensembl transcript: ENST00000528082
  gene symbol: PRCP
  hgvsc: ENST00000528082.1:c.56A>G
  hgvsp: ENSP00000435071.1:p.Tyr19Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000317362
  ensembl transcript: ENST00000313010
  gene symbol: PRCP
  hgvsc: ENST00000313010.3:c.371A>G
  hgvsp: ENSP00000317362.3:p.Tyr124Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000436095
  ensembl transcript: ENST00000534264
  gene symbol: PRCP
  hgvsc: ENST00000534264.1:c.56A>G
  hgvsp: ENSP00000436095.1:p.Tyr19Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431435
  ensembl transcript: ENST00000531128
  gene symbol: PRCP
  hgvsc: ENST00000531128.1:c.56A>G
  hgvsp: ENSP00000431435.1:p.Tyr19Cys
  variant of: http://identifiers.org/hgnc/9344
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000137509
  ensembl protein: ENSP00000431559
  ensembl transcript: ENST00000534631
  gene symbol: PRCP
  hgvsc: ENST00000534631.1:c.56A>G
  hgvsp: ENSP00000431559.1:p.Tyr19Cys
  variant of: http://identifiers.org/hgnc/9344
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2855
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45872
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Tyr145Cys
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 101
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8629
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 157
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 443
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 114
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 144
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1062
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.283e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.32e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.563e1

DP
type: SiteQuality
SIO_000300: 1.35246e5

QD
type: SiteQuality
SIO_000300: 2.236e1

GenotypeQuality
all individuals: 2820
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4252
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1084
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 778
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 906
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1176
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8322
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3476
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5200
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1956
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4788
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1521
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.021867974657674e-4
allele num: 9786
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63822
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11300
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10156
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.34e-1

QD
type: SiteQuality
SIO_000300: 9.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

DP
type: SiteQuality
SIO_000300: 1.946379e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 518
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11666
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 521
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4824
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 512
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17465
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 2349
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 324
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5443
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2873
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3598
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4387
bin: 8.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11326
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8422
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.565435190983093e-5
allele num: 63880
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.012350678274954e-4
allele num: 9878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.901e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.45e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.134e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.695e0

FS
type: SiteQuality
SIO_000300: 5.477e0

QD
type: SiteQuality
SIO_000300: 1.316e1

DP
type: SiteQuality
SIO_000300: 1.975497e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.076e0

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

GenotypeQuality
all individuals: 3644
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5569
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4913
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3370
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17507
bin: 9.75e1
variant carriers: 5

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

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

GenotypeQuality
all individuals: 2917
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12681
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4460
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10002
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.763979537837361e-4
allele num: 11338
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.682378648353364e-5
allele num: 64070
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.638e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.15e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

MQ
type: SiteQuality
SIO_000300: 5.984e1

DP
type: SiteQuality
SIO_000300: 1.99285e6

FS
type: SiteQuality
SIO_000300: 4.161e0

QD
type: SiteQuality
SIO_000300: 1.368e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.09e-1

GenotypeQuality
all individuals: 162
bin: 5.25e1
variant carriers: 88

GenotypeQuality
all individuals: 8882
bin: 6.25e1
variant carriers: 43

GenotypeQuality
all individuals: 160
bin: 4.25e1
variant carriers: 77

GenotypeQuality
all individuals: 201
bin: 1.25e1
variant carriers: 54

GenotypeQuality
all individuals: 3167
bin: 7.75e1
variant carriers: 157

GenotypeQuality
all individuals: 2217
bin: 9.25e1
variant carriers: 123

GenotypeQuality
all individuals: 375
bin: 2.5e0
variant carriers: 12

GenotypeQuality
all individuals: 172
bin: 4.75e1
variant carriers: 79

GenotypeQuality
all individuals: 521
bin: 7.5e0
variant carriers: 32

GenotypeQuality
all individuals: 207
bin: 1.75e1
variant carriers: 75

GenotypeQuality
all individuals: 2189
bin: 2.25e1
variant carriers: 103

GenotypeQuality
all individuals: 1966
bin: 7.25e1
variant carriers: 100

GenotypeQuality
all individuals: 325
bin: 2.75e1
variant carriers: 51

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 41

GenotypeQuality
all individuals: 31180
bin: 9.75e1
variant carriers: 21994

GenotypeQuality
all individuals: 2863
bin: 8.25e1
variant carriers: 180

Latino
type: Population
allele count: 3102
allele frequency: 2.727272727272727e-1
allele num: 11374
num of homozygotes: 407

South Asian
type: Population
allele count: 3442
allele frequency: 3.083124328197779e-1
allele num: 11164
num of homozygotes: 486

Other
type: Population
allele count: 179
allele frequency: 2.182926829268293e-1
allele num: 820
num of homozygotes: 19

African
type: Population
allele count: 3591
allele frequency: 3.503414634146341e-1
allele num: 10250
num of homozygotes: 640

European (Finnish)
type: Population
allele count: 1134
allele frequency: 1.721834193744306e-1
allele num: 6586
num of homozygotes: 89

European (Non-Finnish)
type: Population
allele count: 12973
allele frequency: 2.013628038369602e-1
allele num: 64426
num of homozygotes: 1342

East Asian
type: Population
allele count: 1370
allele frequency: 1.609114399812074e-1
allele num: 8514
num of homozygotes: 119

VQSLOD
type: SiteQuality
SIO_000300: 6.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.56e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.08e-1

DP
type: SiteQuality
SIO_000300: 2.415455e6

MQRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.04e-1

QD
type: SiteQuality
SIO_000300: 1.701e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.99e0

GenotypeQuality
all individuals: 55
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4708
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5595
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2778
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18021
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 711
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 548
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GenotypeQuality
all individuals: 158
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12838
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variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4399
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 408
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3664
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11422
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.169864295741694e-4
allele num: 8548
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11268
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.829e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.04e0

FS
type: SiteQuality
SIO_000300: 8.021000000000001e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.955e0

DP
type: SiteQuality
SIO_000300: 2.114132e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.591e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.587e1

GenotypeQuality
all individuals: 404
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4699
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 532
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variant carriers: 0

GenotypeQuality
all individuals: 59
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variant carriers: 0

GenotypeQuality
all individuals: 4390
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2343
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2881
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
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variant carriers: 0

GenotypeQuality
all individuals: 550
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variant carriers: 0

GenotypeQuality
all individuals: 3662
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
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variant carriers: 0

GenotypeQuality
all individuals: 12862
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variant carriers: 0

GenotypeQuality
all individuals: 85
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variant carriers: 0

GenotypeQuality
all individuals: 700
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5593
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.25e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64570
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.885729518393461e-5
allele num: 11254
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 1.26e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e-1

QD
type: SiteQuality
SIO_000300: 2.584e1

MQRankSum
type: SiteQuality
SIO_000300: 3.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.71e-1

FS
type: SiteQuality
SIO_000300: 2.147e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-1

DP
type: SiteQuality
SIO_000300: 2.114655e6

MQ
type: SiteQuality
SIO_000300: 6.015e1

GenotypeQuality
all individuals: 211
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2935
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
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variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4696
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13046
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18021
bin: 9.75e1
variant carriers: 10

GenotypeQuality
all individuals: 2894
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5602
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2342
bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11426
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.546886118243975e-4
allele num: 64646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11350
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8560
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

QD
type: SiteQuality
SIO_000300: 1.409e1

DP
type: SiteQuality
SIO_000300: 2.11743e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.830000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 1.854e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQ
type: SiteQuality
SIO_000300: 5.931e1

GenotypeQuality
all individuals: 292
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 123
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5627
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2904
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3662
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4699
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18013
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4391
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3008
bin: 2.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.541212009123975e-5
allele num: 64884
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11816
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.33e0

QD
type: SiteQuality
SIO_000300: 1.634e1

MQRankSum
type: SiteQuality
SIO_000300: -2.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.693e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.99e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.124948e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.08e-1

GenotypeQuality
all individuals: 675
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 94
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4699
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18013
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 124
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3662
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4389
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2900
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3041
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 5.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.081854043392505e-5
allele num: 64896
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11924
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.126405e6

MQRankSum
type: SiteQuality
SIO_000300: 5.74e-1

QD
type: SiteQuality
SIO_000300: 1.505e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.01e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.86e-1

GenotypeQuality
all individuals: 123
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5626
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4699
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2344
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 674
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 390
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2898
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3023
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18012
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3662
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4388
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13636
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10282
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11938
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.54054720236628e-5
allele num: 64912
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.820000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.12e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.01e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.967e0

FS
type: SiteQuality
SIO_000300: 4.908e0

QD
type: SiteQuality
SIO_000300: 9.67e0

DP
type: SiteQuality
SIO_000300: 2.127118e6

GenotypeQuality
all individuals: 62
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2905
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2901
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18011
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 118
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13861
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 523
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4390
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3660
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5635
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4700
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2342
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65014
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12272
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

VQSLOD
type: SiteQuality
SIO_000300: 7.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.225e0

QD
type: SiteQuality
SIO_000300: 1.064e1

MQ
type: SiteQuality
SIO_000300: 5.937e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.91e-1

FS
type: SiteQuality
SIO_000300: 6.3e-1

DP
type: SiteQuality
SIO_000300: 2.130879e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.77e-1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 2901
bin: 2.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.538130248869474e-5
allele num: 65014
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.9e-2

MQ
type: SiteQuality
SIO_000300: 5.937e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.91e-1

FS
type: SiteQuality
SIO_000300: 6.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.225e0

QD
type: SiteQuality
SIO_000300: 1.064e1

MQRankSum
type: SiteQuality
SIO_000300: 1.57e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

DP
type: SiteQuality
SIO_000300: 2.130879e6

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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bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65040
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 12374
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8630
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.715356458079135e-5
allele num: 11474
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 846
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.924e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.473e0

FS
type: SiteQuality
SIO_000300: 9.225e0

QD
type: SiteQuality
SIO_000300: 1.668e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.49e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.47e0

DP
type: SiteQuality
SIO_000300: 2.133338e6

VQSLOD
type: SiteQuality
SIO_000300: -1.407e0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.698677800974252e-5
allele num: 11496
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13256
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.062e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.46e-1

QD
type: SiteQuality
SIO_000300: 1.391e1

DP
type: SiteQuality
SIO_000300: 2.145323e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.467e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.839e0

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10334
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65432
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11496
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.499625018749062e-5
allele num: 13334
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.111e0

MQRankSum
type: SiteQuality
SIO_000300: -3.11e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.41e-1

DP
type: SiteQuality
SIO_000300: 2.146361e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.73e0

QD
type: SiteQuality
SIO_000300: 1.43e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.51e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65602
num of homozygotes: 0

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

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13910
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.964e1

FS
type: SiteQuality
SIO_000300: 6.3e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.08e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.155404e6

BaseQRankSum
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SIO_000300: 3.35e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.4e-2

QD
type: SiteQuality
SIO_000300: 1.3e1

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
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65678
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14070
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele count: 1
allele frequency: 8.688097306689835e-5
allele num: 11510
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.61e0

FS
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QD
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MQRankSum
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MQ
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SIO_000300: 5.938e1

BaseQRankSum
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DP
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ReadPosRankSum
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SIO_000300: -1.534e0

VQSLOD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 7.7e-3

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.509023963300537e-5
allele num: 66268
num of homozygotes: 0

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

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

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

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

South Asian
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allele count: 7
allele frequency: 4.473986961523712e-4
allele num: 15646
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.958e0

ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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QD
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BaseQRankSum
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VQSLOD
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DP
type: SiteQuality
SIO_000300: 2.185974e6

MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeQuality
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variant carriers: 0

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

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

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

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

Latino
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European (Non-Finnish)
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allele frequency: 6.02990834539315e-5
allele num: 66336
num of homozygotes: 0

East Asian
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South Asian
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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DP
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SIO_000300: 2.187172e6

QD
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MQRankSum
type: SiteQuality
SIO_000300: -4.1e-2

GenotypeQuality
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variant carriers: 1

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

European (Finnish)
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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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European (Non-Finnish)
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allele num: 66474
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Latino
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East Asian
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Other
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BaseQRankSum
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MQ
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QD
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MQRankSum
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FS
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DP
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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South Asian
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Latino
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502178158329578e-5
allele num: 66570
num of homozygotes: 0

South Asian
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num of homozygotes: 0

East Asian
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 900
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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ClippingRankSum
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SIO_000300: -2.2e-1

ReadPosRankSum
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MQ
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DP
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VQSLOD
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QD
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InbreedingCoeff
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SIO_000300: 1.9e-2

BaseQRankSum
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FS
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MQRankSum
type: SiteQuality
SIO_000300: 9.62e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

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

European (Non-Finnish)
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allele frequency: 1.502178158329578e-5
allele num: 66570
num of homozygotes: 0

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Other
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allele num: 906
num of homozygotes: 0

Latino
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allele num: 11562
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South Asian
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East Asian
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ReadPosRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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FS
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DP
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VQSLOD
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

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

European (Finnish)
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Latino
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Other
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South Asian
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European (Non-Finnish)
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allele num: 66602
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African
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MQ
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QD
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FS
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BaseQRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66606
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: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
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DP
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QD
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SIO_000300: 1.411e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
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

East Asian
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Other
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num of homozygotes: 0

South Asian
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FS
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ReadPosRankSum
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VQSLOD
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MQRankSum
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QD
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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MQ
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DP
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SIO_000300: 2.19935e6

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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South Asian
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African
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East Asian
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European (Finnish)
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num of homozygotes: 0

ReadPosRankSum
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MQRankSum
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BaseQRankSum
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ClippingRankSum
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DP
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MQ
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VQSLOD
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InbreedingCoeff
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FS
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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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 906
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

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

Latino
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allele frequency: 0.0e0
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South Asian
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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African
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QD
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MQRankSum
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VQSLOD
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BaseQRankSum
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MQ
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ClippingRankSum
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FS
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DP
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ReadPosRankSum
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InbreedingCoeff
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

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

East Asian
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 frequency: 0.0e0
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South Asian
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allele num: 16076
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East Asian
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European (Finnish)
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allele frequency: 0.0e0
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African
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Other
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BaseQRankSum
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MQ
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ReadPosRankSum
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FS
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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South Asian
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Latino
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European (Finnish)
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European (Non-Finnish)
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Other
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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QD
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FS
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DP
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MQ
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ClippingRankSum
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MQRankSum
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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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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num of homozygotes: 0

South Asian
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num of homozygotes: 0

European (Finnish)
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East Asian
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Other
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InbreedingCoeff
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MQ
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ReadPosRankSum
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MQRankSum
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VQSLOD
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BaseQRankSum
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FS
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DP
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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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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InbreedingCoeff
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ClippingRankSum
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DP
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BaseQRankSum
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QD
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VQSLOD
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MQRankSum
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MQ
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FS
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66172
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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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South Asian
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FS
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BaseQRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQRankSum
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QD
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DP
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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Latino
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European (Finnish)
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QD
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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MQ
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MQRankSum
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FS
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ClippingRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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num of homozygotes: 0

South Asian
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allele frequency: 7.108330963889678e-5
allele num: 14068
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 count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

ClippingRankSum
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FS
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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MQRankSum
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QD
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MQ
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SIO_000300: 5.959e1

DP
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SIO_000300: 2.142465e6

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65302
num of homozygotes: 0

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele frequency: 1.161170459823502e-4
allele num: 8612
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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BaseQRankSum
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SIO_000300: -1.286e0

ReadPosRankSum
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ClippingRankSum
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FS
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DP
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VQSLOD
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InbreedingCoeff
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SIO_000300: -5.999999999999999e-4

MQ
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SIO_000300: 6.0e1

MQRankSum
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SIO_000300: 2.23e0

QD
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SIO_000300: 1.426e1

GenotypeDepth
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variant carriers: 0

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

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
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num of homozygotes: 0

South Asian
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allele num: 12828
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64914
num of homozygotes: 0

East Asian
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allele count: 0
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
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SIO_000300: 2.111586e6

InbreedingCoeff
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SIO_000300: -1.1e-3

ClippingRankSum
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MQRankSum
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 1.833e0

VQSLOD
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SIO_000300: 7.6e-3

MQ
type: SiteQuality
SIO_000300: 5.975e1

QD
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SIO_000300: 1.639e1

GenotypeDepth
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64490
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 9990
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11430
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

Other
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num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 8.379420144126027e-5
allele num: 11934
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.09666e6

BaseQRankSum
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SIO_000300: -3.68e0

ReadPosRankSum
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SIO_000300: 1.06e0

MQ
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InbreedingCoeff
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SIO_000300: -2.0e-3

ClippingRankSum
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SIO_000300: -1.489e0

FS
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SIO_000300: 1.944e0

MQRankSum
type: SiteQuality
SIO_000300: 7.48e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.32e-1

QD
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GenotypeDepth
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

East Asian
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allele count: 2
allele frequency: 2.340276152586005e-4
allele num: 8546
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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African
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European (Non-Finnish)
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allele num: 64386
num of homozygotes: 0

ReadPosRankSum
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MQ
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BaseQRankSum
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MQRankSum
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VQSLOD
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FS
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QD
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InbreedingCoeff
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ClippingRankSum
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DP
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GenotypeDepth
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variant carriers: 3

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

South Asian
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allele frequency: 8.592541673827119e-5
allele num: 11638
num of homozygotes: 0

European (Finnish)
type: Population
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allele frequency: 0.0e0
allele num: 6602
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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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East Asian
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allele frequency: 4.098360655737705e-3
allele num: 8540
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.109936246306951e-5
allele num: 64310
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VQSLOD
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MQ
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DP
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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FS
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BaseQRankSum
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 63748
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South 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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FS
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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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MQRankSum
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ReadPosRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 5
allele frequency: 4.782858236081883e-4
allele num: 10454
num of homozygotes: 0

European (Non-Finnish)
type: Population
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allele frequency: 0.0e0
allele num: 63630
num of homozygotes: 0

African
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European (Finnish)
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Other
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Latino
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allele frequency: 0.0e0
allele num: 11356
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.057591e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.900000000000001e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.57e-1

BaseQRankSum
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SIO_000300: 4.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.649e1

GenotypeDepth
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 7.5e0
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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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bin: 8.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1022
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63382
num of homozygotes: 0

African
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allele count: 2
allele frequency: 2.054231717337716e-4
allele num: 9736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8448
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.187e0

QD
type: SiteQuality
SIO_000300: 1.501e1

VQSLOD
type: SiteQuality
SIO_000300: -3.61e-2

MQRankSum
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SIO_000300: -1.532e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -7.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.33e0

DP
type: SiteQuality
SIO_000300: 2.049336e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

GenotypeDepth
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10160
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 792
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9730
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.648305084745763e-4
allele num: 11328
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63390
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.63e-1

BaseQRankSum
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SIO_000300: -2.59e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.96e-1

FS
type: SiteQuality
SIO_000300: 6.233e0

DP
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SIO_000300: 2.048396e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.6e-2

QD
type: SiteQuality
SIO_000300: 1.516e1

VQSLOD
type: SiteQuality
SIO_000300: 4.03e-1

GenotypeDepth
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7885
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 241
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GenotypeQuality
all individuals: 745
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8058
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50430
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.591861524445795e-5
allele num: 13172
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5810
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6492
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.087589e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.733e0

QD
type: SiteQuality
SIO_000300: 1.314e1

MQRankSum
type: SiteQuality
SIO_000300: -6.66e-1

ReadPosRankSum
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SIO_000300: -1.466e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.2e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.575e-1

GenotypeDepth
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8974
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.21654501216545e-4
allele num: 8220
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 730
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5834
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51124
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

VQSLOD
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ClippingRankSum
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MQ
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SIO_000300: 5.909e1

FS
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SIO_000300: 0.0e0

MQRankSum
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ReadPosRankSum
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SIO_000300: -2.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.98e0

DP
type: SiteQuality
SIO_000300: 1.137457e6

QD
type: SiteQuality
SIO_000300: 1.219e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1992
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54300
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.147052076164258e-4
allele num: 8718
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9542
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5996
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.252118e6

ClippingRankSum
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QD
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VQSLOD
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FS
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SIO_000300: 3.188e0

ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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SIO_000300: 3.67e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8862
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 55452
num of homozygotes: 0

European (Finnish)
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allele count: 0
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Other
type: Population
allele count: 0
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South Asian
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allele frequency: 7.155123068116771e-5
allele num: 13976
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BaseQRankSum
type: SiteQuality
SIO_000300: -9.22e-1

ClippingRankSum
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DP
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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FS
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.202e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1417
bin: 2.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6218
num of homozygotes: 0

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

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

Other
type: Population
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African
type: Population
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allele frequency: 1.078515962036238e-4
allele num: 9272
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58514
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.836000000000001e-1

FS
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ClippingRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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MQRankSum
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MQ
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SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.881e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.86e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

East Asian
type: Population
allele count: 1
allele frequency: 1.304461257500652e-4
allele num: 7666
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 836
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 59616
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6282
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.98e-1

BaseQRankSum
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ReadPosRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: -9.0e-4

FS
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DP
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QD
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SIO_000300: 1.357e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10966
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9938
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.158859020121932e-5
allele num: 63314
num of homozygotes: 0

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: 8174
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

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

QD
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SIO_000300: 1.831e1

MQRankSum
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FS
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InbreedingCoeff
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DP
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MQ
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 8.110000000000001e-1

VQSLOD
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SIO_000300: 6.66e-1

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15836
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.189343482397717e-4
allele num: 8408
num of homozygotes: 0

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

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 64652
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6516
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
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ReadPosRankSum
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DP
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SIO_000300: 1.473641e6

InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 1.8e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.15e-1

BaseQRankSum
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SIO_000300: -9.54e-1

GenotypeDepth
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16408
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66406
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.22e-1

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502629601803156e-5
allele num: 66550
num of homozygotes: 0

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

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

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

Other
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num of homozygotes: 0

ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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FS
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BaseQRankSum
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MQ
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DP
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SIO_000300: 1.517814e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 1.925669170036588e-4
allele num: 10386
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11526
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

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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East Asian
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South Asian
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QD
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InbreedingCoeff
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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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BaseQRankSum
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VQSLOD
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
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num of homozygotes: 0

Other
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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

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

East Asian
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DP
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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FS
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SIO_000300: 2.67e0

MQ
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SIO_000300: 6.0e1

QD
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SIO_000300: 1.464e1

ReadPosRankSum
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SIO_000300: 1.26e0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.50177209106746e-5
allele num: 66588
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 8642
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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MQRankSum
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DP
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MQ
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FS
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SIO_000300: 8.51e-1

QD
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BaseQRankSum
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SIO_000300: 2.73e-1

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

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

East Asian
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num of homozygotes: 0

Other
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European (Non-Finnish)
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allele num: 66614
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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DP
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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FS
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SIO_000300: 1.174e0

VQSLOD
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MQRankSum
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SIO_000300: 3.96e-1

QD
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SIO_000300: 1.148e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66620
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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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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Other
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ReadPosRankSum
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DP
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ClippingRankSum
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VQSLOD
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MQ
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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