22-22020370-T-TCGC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22020370
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22020373
    reference: chr 22
allele count: 1
allele frequency: 9.363295880149813e-6
allele num: 106800
alternate allele: TCGC
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.-9_-7dupCGC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.-9_-7dupCGC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.-9_-7dupCGC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.13_15dupCGC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.-9_-7dupCGC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.-9_-7dupCGC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.-9_-7dupCGC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.-9_-7dupCGC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-3822_769-3820dupCGC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.63_65dupCGC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.83_85dupCGC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.-9_-7dupCGC
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6873
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28437
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11151
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5934
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum

22-22020375-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22020375
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22020375
    reference: chr 22
allele count: 2
allele frequency: 1.864141376481992e-5
allele num: 107288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.8G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.-14G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.-14G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.-14G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-3827G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.78G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.-14G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.-14G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.-14G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.-14G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.-14G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.58G>A
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5710
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5680
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2170
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2099
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12095
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29853
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

22-22020382-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22020382
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22020382
    reference: chr 22
allele count: 2
allele frequency: 1.817785210499527e-5
allele num: 110024
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.15C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.-7C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-3820C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.-7C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.85C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.-7C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.-7C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.-7C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.-7C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.-7C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.-7C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.65C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13304
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32758
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

22-22020413-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22020413
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22020413
    reference: chr 22
allele count: 2
allele frequency: 1.868704800702633e-5
allele num: 107026
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.25G>C
  hgvsp: ENSP00000334553.7:p.Asp9His
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.25G>C
  hgvsp: ENSP00000406745.1:p.Asp9His
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.25G>C
  hgvsp: ENSP00000395181.1:p.Asp9His
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.25G>C
  hgvsp: ENSP00000381812.3:p.Asp9His
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.25G>C
  hgvsp: ENSP00000384299.1:p.Asp9His
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.25G>C
  hgvsp: ENSP00000445312.1:p.Asp9His
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.116G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-3789G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.46G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.25G>C
  hgvsp: ENSP00000390427.1:p.Asp9His
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.25G>C
  hgvsp: ENSP00000396228.2:p.Asp9His
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.96G>C
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2415
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6740
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6235
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14642
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27110
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp9His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD

22-22020420-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22020420
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22020420
    reference: chr 22
allele count: 1
allele frequency: 9.679417686231996e-6
allele num: 103312
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.32T>C
  hgvsp: ENSP00000445312.1:p.Met11Thr
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.32T>C
  hgvsp: ENSP00000406745.1:p.Met11Thr
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.32T>C
  hgvsp: ENSP00000334553.7:p.Met11Thr
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.32T>C
  hgvsp: ENSP00000396228.2:p.Met11Thr
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.32T>C
  hgvsp: ENSP00000390427.1:p.Met11Thr
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.123T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.32T>C
  hgvsp: ENSP00000395181.1:p.Ile11Thr
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.103T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-3782T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.53T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.32T>C
  hgvsp: ENSP00000384299.1:p.Met11Thr
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.32T>C
  hgvsp: ENSP00000381812.3:p.Met11Thr
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9981
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21969
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8384
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met11Thr
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

22-22020426-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22020426
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22020426
    reference: chr 22
allele count: 7
allele frequency: 7.036165892688418e-5
allele num: 99486
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.32+6T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.32+6T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.103+6T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.32+6T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.53+6T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-3776T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.123+6T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.32+6T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.32+6T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.32+6T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.32+6T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.32+6T>C
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9940
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11319
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2583
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14873
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16751
  bin: 2.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: c.32+6T>C
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ

22-22020428-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22020428
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22020428
    reference: chr 22
allele count: 1
allele frequency: 1.016962941870398e-5
allele num: 98332
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.32+8G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.123+8G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.103+8G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.32+8G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.32+8G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.32+8G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.32+8G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.32+8G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-3774G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.53+8G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.32+8G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.32+8G>C
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10321
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15167
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16525
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.32+8G>C
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

22-22020430-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22020430
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22020430
    reference: chr 22
allele count: 1
allele frequency: 1.037818091244967e-5
allele num: 96356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.32+10G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.103+10G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.32+10G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.32+10G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.32+10G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.32+10G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.123+10G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.32+10G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.32+10G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.53+10G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.32+10G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-3772G>C
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3515
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1372
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12556
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9174
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

22-22020432-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22020432
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22020432
    reference: chr 22
allele count: 2
allele frequency: 2.095030587446577e-5
allele num: 95464
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-3770C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.103+12C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.53+12C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.32+12C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.32+12C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.32+12C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.32+12C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.32+12C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.123+12C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.32+12C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.32+12C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.32+12C>G
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8703
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11579
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20097
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11047
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

22-22020432-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22020432
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22020432
    reference: chr 22
allele count: 2
allele frequency: 2.095030587446577e-5
allele num: 95464
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.32+12C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.32+12C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.32+12C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.32+12C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.123+12C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.53+12C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-3770C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.32+12C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.32+12C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.32+12C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.103+12C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.32+12C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20097
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11047
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8703
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3696
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

22-22020437-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22020437
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22020437
    reference: chr 22
allele count: 1
allele frequency: 1.084434033877719e-5
allele num: 92214
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.32+17T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.32+17T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.32+17T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.32+17T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-3765T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.123+17T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.32+17T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.32+17T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.32+17T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.53+17T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.32+17T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.103+17T>A
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23043
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8675
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4379
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11915
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6752
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1394
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum

22-22020439-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22020439
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22020439
    reference: chr 22
allele count: 2
allele frequency: 2.213466731595024e-5
allele num: 90356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.32+19G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.53+19G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.32+19G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-3763G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.32+19G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.32+19G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.32+19G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.103+19G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.123+19G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.32+19G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.32+19G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.32+19G>A
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5864
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4775
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7654
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23930
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD

22-22020440-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22020440
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22020440
    reference: chr 22
allele count: 1
allele frequency: 1.110494169905608e-5
allele num: 90050
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.32+20G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-3762G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.123+20G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.32+20G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.32+20G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.103+20G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.32+20G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.53+20G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.32+20G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.32+20G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.32+20G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.32+20G>A
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5672
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4790
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

22-22020471-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22020471
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22020471
    reference: chr 22
allele count: 6
allele frequency: 8.529269610212379e-5
allele num: 70346
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.53+51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.32+51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.32+51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.32+51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.32+51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-3731G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.123+51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.32+51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.32+51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.32+51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.103+51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.32+51G>A
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 464
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19500
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4326
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7860
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3336
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20832
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1785
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff

22-22023603-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22023603
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22023603
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 3938
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-599A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-599A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.33-20A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-599A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-599A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-599A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-599A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-599A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-599A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-599A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-599A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-599A>G
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2262
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3012
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1117
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

22-22023617-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22023617
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22023617
    reference: chr 22
allele count: 1
allele frequency: 1.655629139072848e-4
allele num: 6040
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-585T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-585T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-585T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-585T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-585T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-585T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-585T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-585T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-585T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.33-6T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-585T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-585T>C
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1900
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.33-6T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: African
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

22-22023621-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22023621
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22023621
    reference: chr 22
allele count: 42
allele frequency: 6.169212690951821e-3
allele num: 6808
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-581A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-581A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-581A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-581A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-581A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-581A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.33-2A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-581A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-581A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-581A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-581A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-581A>G
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2349
  bin: 2.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2053
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 2.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: c.33-2A>G
num of homozygotes: 2
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

22-22023635-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22023635
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22023635
    reference: chr 22
allele count: 1
allele frequency: 1.149425287356322e-4
allele num: 8700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-567G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-567G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-567G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-567G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.45G>T
  hgvsp: ENST00000458567.1:c.45G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-567G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-567G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-567G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-567G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-567G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-567G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-567G>T
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3326
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser15Ser
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

22-22023637-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22023637
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22023637
    reference: chr 22
allele count: 1
allele frequency: 1.127649977447e-4
allele num: 8868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-565T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-565T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-565T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.47T>C
  hgvsp: ENSP00000395181.1:p.Leu16Pro
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-565T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-565T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-565T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-565T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-565T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-565T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-565T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-565T>C
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2094
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 627
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu16Pro
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: MQRankSum

22-22023646-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22023646
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22023646
    reference: chr 22
allele count: 1
allele frequency: 1.071122536418166e-4
allele num: 9336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-556C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-556C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.56C>G
  hgvsp: ENSP00000395181.1:p.Pro19Arg
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-556C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-556C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-556C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-556C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-556C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-556C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-556C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-556C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-556C>G
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro19Arg
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

22-22023646-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22023646
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22023646
    reference: chr 22
allele count: 3
allele frequency: 3.213367609254498e-4
allele num: 9336
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-556C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-556C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-556C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-556C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-556C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-556C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-556C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.56C>T
  hgvsp: ENSP00000395181.1:p.Pro19Leu
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-556C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-556C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-556C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-556C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2185
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3612
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro19Leu
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff

22-22023677-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22023677
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22023677
    reference: chr 22
allele count: 2
allele frequency: 2.184837229626393e-4
allele num: 9154
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-525A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-525A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-525A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-525A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-525A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-525A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.87A>G
  hgvsp: ENST00000458567.1:c.87A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-525A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-525A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-525A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-525A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-525A>G
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2388
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 891
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2930
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln29Gln
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

22-22023682-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22023682
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22023682
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 8850
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.92C>T
  hgvsp: ENSP00000395181.1:p.Ser31Phe
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-520C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-520C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-520C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-520C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-520C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-520C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-520C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-520C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-520C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-520C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-520C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 2357
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser31Phe
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: DP

22-22023737-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22023737
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22023737
    reference: chr 22
allele count: 1
allele frequency: 1.691474966170501e-4
allele num: 5912
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-465C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-465C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-465C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-465C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-465C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-465C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.125+22C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-465C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-465C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-465C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-465C>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-465C>G
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3277
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

22-22023748-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22023748
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22023748
    reference: chr 22
allele count: 1
allele frequency: 1.804402742692169e-4
allele num: 5542
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-454T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.125+33T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-454T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-454T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-454T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-454T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-454T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-454T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-454T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-454T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-454T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-454T>C
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2102
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3490
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

22-22024151-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024151
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024151
    reference: chr 22
allele count: 3
allele frequency: 2.471576866040534e-5
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.126-51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-51G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-51G>A
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4028
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2935
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6932
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18281
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP

22-22024153-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024153
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024153
    reference: chr 22
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-49C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-49C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-49C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-49C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.126-49C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-49C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-49C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-49C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-49C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-49C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-49C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-49C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18296
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6930
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1289
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3957
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 927
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP

22-22024156-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024156
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024156
    reference: chr 22
allele count: 26
allele frequency: 2.141962696895802e-4
allele num: 121384
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-46C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-46C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-46C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-46C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-46C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-46C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-46C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-46C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.126-46C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-46C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-46C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-46C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18305
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1967
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13931
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

22-22024163-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024163
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024163
    reference: chr 22
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-39A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.126-39A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-39A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-39A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-39A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-39A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-39A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-39A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-39A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-39A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-39A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-39A>G
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6927
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13939
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: MQ

22-22024166-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024166
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024166
    reference: chr 22
allele count: 5
allele frequency: 4.11936265221045e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-36G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-36G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-36G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-36G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-36G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-36G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-36G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.126-36G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-36G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-36G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-36G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-36G>A
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13935
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2644
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2928
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP

22-22024169-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024169
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024169
    reference: chr 22
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-33G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.126-33G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-33G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-33G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-33G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-33G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-33G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-33G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-33G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-33G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-33G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-33G>T
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18323
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2927
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

22-22024185-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024185
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024185
    reference: chr 22
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.126-17C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-17C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-17C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-17C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-17C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-17C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-17C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-17C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-17C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-17C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-17C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-17C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13932
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18330
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2641
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: MQ

22-22024194-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024194
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024194
    reference: chr 22
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-8T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-8T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-8T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-8T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-8T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.126-8T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-8T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-8T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-8T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-8T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-8T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-8T>G
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18332
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2642
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.33-8T>G
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
reference allele: T
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

22-22024196-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024196
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024196
    reference: chr 22
allele count: 9
allele frequency: 7.414974953862378e-5
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.33-6C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.124-6C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.33-6C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.33-6C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.33-6C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.33-6C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.33-6C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.33-6C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.104-6C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.126-6C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.769-6C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.54-6C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1645
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2639
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4108
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.33-6C>T
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

22-22024211-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024211
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024211
    reference: chr 22
allele count: 2
allele frequency: 1.647853670594051e-5
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.42C>T
  hgvsp: ENST00000335025.8:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.135C>T
  hgvsp: ENST00000458567.1:c.135C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.133C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.42C>T
  hgvsp: ENST00000417788.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.42C>T
  hgvsp: ENST00000492445.2:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.42C>T
  hgvsp: ENST00000412327.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.63C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.42C>T
  hgvsp: ENST00000398831.3:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.778C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.42C>T
  hgvsp: ENST00000406385.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.42C>T
  hgvsp: ENST00000456792.2:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.113C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2926
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1966
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13919
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18341
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr14Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ

22-22024212-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024212
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024212
    reference: chr 22
allele count: 3
allele frequency: 2.471780505891077e-5
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.43T>A
  hgvsp: ENSP00000384299.1:p.Cys15Ser
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.136T>A
  hgvsp: ENSP00000395181.1:p.Cys46Ser
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.43T>A
  hgvsp: ENSP00000390427.1:p.Cys15Ser
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.779T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.43T>A
  hgvsp: ENSP00000334553.7:p.Cys15Ser
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.64T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.43T>A
  hgvsp: ENSP00000396228.2:p.Cys15Ser
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.43T>A
  hgvsp: ENSP00000406745.1:p.Cys15Ser
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.43T>A
  hgvsp: ENSP00000445312.1:p.Cys15Ser
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.43T>A
  hgvsp: ENSP00000381812.3:p.Cys15Ser
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.134T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.114T>A
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18337
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3946
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Cys15Ser
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: African
reference allele: T
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

22-22024223-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024223
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024223
    reference: chr 22
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.147C>T
  hgvsp: ENST00000458567.1:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.54C>T
  hgvsp: ENST00000492445.2:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.54C>T
  hgvsp: ENST00000406385.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.54C>T
  hgvsp: ENST00000335025.8:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.54C>T
  hgvsp: ENST00000417788.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.790C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.125C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.54C>T
  hgvsp: ENST00000412327.1:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.75C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.54C>T
  hgvsp: ENST00000398831.3:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.145C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.54C>T
  hgvsp: ENST00000456792.2:c.54C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2640
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18331
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr18Tyr
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: East Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff

22-22024252-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024252
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024252
    reference: chr 22
allele count: 1
allele frequency: 8.243887157672586e-6
allele num: 121302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.175+1G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.103+1G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.82+1G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.82+1G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.174G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.82+1G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.82+1G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.82+1G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.82+1G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.819G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.153+1G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: splice_donor_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.82+1G>A
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2636
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4117
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3940
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13822
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.82+1G>A
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP

22-22024254-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024254
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024254
    reference: chr 22
allele count: 1
allele frequency: 8.244566830458728e-6
allele num: 121292
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.82+3A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.82+3A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.82+3A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.82+3A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.153+3A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.82+3A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.103+3A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.176A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.82+3A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.82+3A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.821A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.175+3A>G
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4120
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2635
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6895
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18219
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.82+3A>G
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ

22-22024259-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024259
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024259
    reference: chr 22
allele count: 1
allele frequency: 8.246062505153789e-6
allele num: 121270
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.82+8A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.103+8A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.82+8A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.82+8A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.82+8A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.82+8A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.82+8A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.82+8A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.153+8A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.826A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.181A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.175+8A>G
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2633
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6883
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18170
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.82+8A>G
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

22-22024266-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024266
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024266
    reference: chr 22
allele count: 1
allele frequency: 8.249463784853985e-6
allele num: 121220
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.188C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.175+15C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.82+15C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.153+15C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.82+15C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.833C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.82+15C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.82+15C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.82+15C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.103+15C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.82+15C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.82+15C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13665
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6861
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18002
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2926
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

22-22024267-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024267
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024267
    reference: chr 22
allele count: 1
allele frequency: 8.249463784853985e-6
allele num: 121220
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.82+16T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.82+16T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.82+16T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.189T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.834T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.175+16T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.103+16T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.82+16T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.82+16T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.82+16T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.153+16T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.82+16T>G
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3922
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4087
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1962
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13656
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6857
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1647
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

22-22024274-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024274
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024273
    reference: chr 22
allele count: 92
allele frequency: 7.597278192508423e-4
allele num: 121096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.153+27delC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.82+27delC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.82+27delC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.82+27delC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.82+27delC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.82+27delC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.82+27delC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.200delC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.845delC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.82+27delC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.103+27delC
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.175+27delC
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6784
  bin: 3.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3898
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13267
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 17484
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2625
  bin: 4.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1281
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: TC
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP

22-22024276-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024276
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024276
    reference: chr 22
allele count: 1
allele frequency: 8.271709100534353e-6
allele num: 120894
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.175+25C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.82+25C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.153+25C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.82+25C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.198C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.82+25C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.82+25C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.103+25C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.82+25C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.843C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.82+25C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.82+25C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 895
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1947
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1644
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3887
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6745
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17267
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13089
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQ

22-22024278-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024278
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024278
    reference: chr 22
allele count: 2
allele frequency: 1.652892561983471e-5
allele num: 121000
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.82+27C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.82+27C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.82+27C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.82+27C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.82+27C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.82+27C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.82+27C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.175+27C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.845C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.200C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.153+27C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.103+27C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6702
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4147
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2609
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 670
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1284
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1945
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17032
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

22-22024279-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024279
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024279
    reference: chr 22
allele count: 21
allele frequency: 1.735336407357826e-4
allele num: 121014
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.153+28G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.82+28G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.82+28G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.82+28G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.82+28G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.201G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.175+28G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.82+28G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.82+28G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.846G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.82+28G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.103+28G>A
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1283
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4209
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3857
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1578
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16810
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6643
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2602
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 12528
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1641
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff

22-22024280-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024280
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024280
    reference: chr 22
allele count: 3
allele frequency: 2.478642364955302e-5
allele num: 121034
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.82+29T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.175+29T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.82+29T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.847T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.202T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.82+29T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.82+29T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.82+29T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.82+29T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.103+29T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.82+29T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.153+29T>C
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6624
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16843
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2599
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: African
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

22-22024281-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024281
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024281
    reference: chr 22
allele count: 26
allele frequency: 2.149008976245185e-4
allele num: 120986
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.848T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.82+30T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.82+30T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.82+30T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.103+30T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.203T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.153+30T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.82+30T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.175+30T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.82+30T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.82+30T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.82+30T>C
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2600
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12169
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6583
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4317
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2924
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16417
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1942
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: QD

22-22024284-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024284
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024284
    reference: chr 22
allele count: 2
allele frequency: 1.653603201375798e-5
allele num: 120948
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.82+33G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.175+33G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.82+33G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.82+33G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.103+33G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.153+33G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.206G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.851G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.82+33G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.82+33G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.82+33G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.82+33G>A
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2922
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1880
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1940
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2690
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3817
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16027
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4456
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

22-22024291-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024291
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024291
    reference: chr 22
allele count: 1
allele frequency: 8.279653579294243e-6
allele num: 120778
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.82+40G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.103+40G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000496819
  gene symbol: PPIL2
  hgvsc: ENST00000496819.1:n.213G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498589
  gene symbol: PPIL2
  hgvsc: ENST00000498589.1:n.858G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.82+40G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.153+40G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.82+40G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.82+40G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.82+40G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.82+40G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.82+40G>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.175+40G>C
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6377
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10498
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5255
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14197
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1639
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5031
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1282
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1939
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2921
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2591
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: Latino
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP

22-22024612-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024612
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024612
    reference: chr 22
allele count: 3
allele frequency: 2.011532787984444e-4
allele num: 14914
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-243T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-243T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-243T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.107T>C
  hgvsp: ENSP00000406745.1:p.Ile36Thr
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-243T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-243T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.213T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-243T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-243T>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-243T>C
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16137
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1381
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4404
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14624
  bin: 7.5e0
  variant carriers: 1
hgvs: p.Ile36Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum

22-22024619-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024619
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024619
    reference: chr 22
allele count: 2
allele frequency: 1.334935255640101e-4
allele num: 14982
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.114A>G
  hgvsp: ENST00000417788.1:c.114A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-236A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-236A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.220A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-236A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-236A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-236A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-236A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-236A>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-236A>G
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17791
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4333
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg38Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

22-22024621-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024621
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024621
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 15000
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.222C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-234C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-234C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-234C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.116C>T
  hgvsp: ENSP00000406745.1:p.Ala39Val
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-234C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-234C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-234C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-234C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-234C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4296
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18276
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16436
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala39Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

22-22024664-CAGTA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024664
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024660
    reference: chr 22
allele count: 1
allele frequency: 6.28140703517588e-5
allele num: 15920
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.266+3_266+6delAAGT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-187_104-184delAAGT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-187_83-184delAAGT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*18+19_*18+22delAAGT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-187_83-184delAAGT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-187_83-184delAAGT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-187_176-184delAAGT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-187_83-184delAAGT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-187_83-184delAAGT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-187_83-184delAAGT
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: splice donor
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6169
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1896
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31289
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2202
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 9.25e1
  variant carriers: 0
hgvs: n.266+3_266+6delAAGT
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: CAGTA
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

22-22024666-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024666
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024666
    reference: chr 22
allele count: 2
allele frequency: 1.245640259093174e-4
allele num: 16056
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: non_coding_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.266+1G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-189G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-189G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-189G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-189G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-189G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-189G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-189G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*18+17G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-189G>T
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31582
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6669
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1702
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 708
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 9.25e1
  variant carriers: 0
hgvs: n.266+1G>T
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/22-22024669-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024669
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024669
    reference: chr 22
allele count: 0
allele frequency: 0.0e0
allele num: 16226
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-186A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.266+4A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-186A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-186A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-186A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-186A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-186A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-186A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-186A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*18+20A>C
  variant of: http://identifiers.org/hgnc/9261
canonical: false
consequence: splice region
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31966
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7690
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1747
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 583
  bin: 4.75e1
  variant carriers: 0
hgvs: n.266+4A>C
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

22-22024805-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024805
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024805
    reference: chr 22
allele count: 1
allele frequency: 8.267605866693123e-6
allele num: 120954
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-50G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-50G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-50G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-50G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-50G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-50G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-50G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*19-50G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-50G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.267-50G>A
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD

22-22024805-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024805
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024805
    reference: chr 22
allele count: 4
allele frequency: 3.307042346677249e-5
allele num: 120954
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-50G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-50G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-50G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-50G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-50G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.267-50G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-50G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*19-50G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-50G>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-50G>T
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4042
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/22-22024810-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024810
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024810
    reference: chr 22
allele count: 1
allele frequency: 8.266512358435975e-6
allele num: 120970
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-45A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-45A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.267-45A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*19-45A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-45A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-45A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-45A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-45A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-45A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-45A>C
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4074
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2645
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 671
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6484
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6068
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1190
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1423
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

22-22024812-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024812
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024812
    reference: chr 22
allele count: 1
allele frequency: 8.265692417053776e-6
allele num: 120982
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-43T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-43T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.267-43T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*19-43T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-43T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-43T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-43T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-43T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-43T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-43T>A
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6491
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 549
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4082
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2289
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/22-22024815-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024815
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024815
    reference: chr 22
allele count: 6
allele frequency: 4.959333465582226e-5
allele num: 120984
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-40A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.267-40A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-40A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-40A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*19-40A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-40A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-40A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-40A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-40A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-40A>C
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2866
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6499
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5643
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 45383
  bin: 9.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

22-22024816-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024816
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024816
    reference: chr 22
allele count: 1
allele frequency: 8.265829062654984e-6
allele num: 120980
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-39C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-39C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-39C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-39C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-39C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-39C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-39C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-39C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*19-39C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.267-39C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6071
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5667
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6504
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4823
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/22-22024817-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024817
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024817
    reference: chr 22
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.267-38A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-38A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-38A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-38A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-38A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-38A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-38A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-38A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*19-38A>C
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-38A>C
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2737
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4121
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6440
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6503
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2086
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

22-22024820-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024820
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024820
    reference: chr 22
allele count: 1
allele frequency: 8.263233568560049e-6
allele num: 121018
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-35G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.267-35G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-35G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-35G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-35G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*19-35G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-35G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-35G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-35G>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-35G>A
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6508
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3056
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 183
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2100
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: DP

22-22024828-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024828
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024828
    reference: chr 22
allele count: 1
allele frequency: 8.257774694875225e-6
allele num: 121098
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-27T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-27T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.267-27T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-27T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-27T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-27T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-27T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-27T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-27T>G
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*19-27T>G
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4217
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5758
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6514
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2454
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1449
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2354
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: DP

22-22024829-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024829
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024829
    reference: chr 22
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-26C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-26C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*19-26C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-26C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-26C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-26C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.267-26C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-26C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-26C>T
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-26C>T
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3230
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6448
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4227
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4043
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1267
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2127
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum

22-22024831-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024831
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024830
    reference: chr 22
allele count: 1
allele frequency: 8.257092842751923e-6
allele num: 121108
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000334553
  ensembl transcript: ENST00000335025
  gene symbol: PPIL2
  hgvsc: ENST00000335025.8:c.83-18delT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-18delT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.267-18delT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-18delT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-18delT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*19-18delT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000390427
  ensembl transcript: ENST00000412327
  gene symbol: PPIL2
  hgvsc: ENST00000412327.1:c.83-18delT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-18delT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-18delT
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000381812
  ensembl transcript: ENST00000398831
  gene symbol: PPIL2
  hgvsc: ENST00000398831.3:c.83-18delT
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1268
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2179
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4237
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6074
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6514
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5776
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2738
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5048
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4824
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1246
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1902
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: GT
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

22-22024848-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 22024848
    reference: chr 22
  end: Position
    type: ExactPosition
    position: 22024848
    reference: chr 22
allele count: 3
allele frequency: 2.473737157181259e-5
allele num: 121274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000395181
  ensembl transcript: ENST00000458567
  gene symbol: PPIL2
  hgvsc: ENST00000458567.1:c.176-7T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000498109
  gene symbol: PPIL2
  hgvsc: ENST00000498109.1:n.104-7T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl transcript: ENST00000484439
  gene symbol: PPIL2
  hgvsc: ENST00000484439.1:n.267-7T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000445312
  ensembl transcript: ENST00000492445
  gene symbol: PPIL2
  hgvsc: ENST00000492445.2:c.83-7T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000396228
  ensembl transcript: ENST00000456792
  gene symbol: PPIL2
  hgvsc: ENST00000456792.2:c.83-7T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000406745
  ensembl transcript: ENST00000417788
  gene symbol: PPIL2
  hgvsc: ENST00000417788.1:c.*19-7T>A
  variant of: http://identifiers.org/hgnc/9261
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000100023
  ensembl protein: ENSP00000384299
  ensembl transcript: ENST00000406385
  gene symbol: PPIL2
  hgvsc: ENST00000406385.1:c.83-7T>A
  variant of: http://identifiers.org/hgnc/9261
canonical: true
consequence: splice region
filter: PASS
hgvs: c.83-7T>A
num of homozygotes: 0
reference allele: T

GenotypeDepth
all individuals: 95
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 980
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2647
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 484
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 250
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 893
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7214
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 520
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35106
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 664
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1963
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1056
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3154
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 387
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1936
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 594
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 58826
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4452
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.143641354071363e-4
allele num: 8744
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 746
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10584
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8066
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.42e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.01e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

DP
type: SiteQuality
SIO_000300: 1.319612e6

QD
type: SiteQuality
SIO_000300: 1.634e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e-1

GenotypeDepth
all individuals: 73
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1361
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1802
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 638
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3306
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6982
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37850
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 486
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 546
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 1.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8776
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4482
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10648
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8066
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.385125757421888e-5
allele num: 59082
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -6.608000000000001e-1

QD
type: SiteQuality
SIO_000300: 7.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

DP
type: SiteQuality
SIO_000300: 1.349786e6

FS
type: SiteQuality
SIO_000300: 6.941e0

MQRankSum
type: SiteQuality
SIO_000300: -5.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.120000000000001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.02e-1

GenotypeDepth
all individuals: 182
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 961
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 912
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42707
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 391
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6754
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 264
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 107
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 170
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3649
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1800
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 601
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4930
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15592
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.189621195533173e-4
allele num: 9134
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10798
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60584
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.77e-1

QD
type: SiteQuality
SIO_000300: 1.052e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.37e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.225e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.83e-1

DP
type: SiteQuality
SIO_000300: 1.400437e6

GenotypeDepth
all individuals: 83
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 127
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 94
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 211
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 869
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1084
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 3268
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39096
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11305
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 7.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.390060343074107e-5
allele num: 58996
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7900
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9026
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15248
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4702
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.01e0

DP
type: SiteQuality
SIO_000300: 1.362058e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

MQ
type: SiteQuality
SIO_000300: 5.969e1

MQRankSum
type: SiteQuality
SIO_000300: 7.28e-1

FS
type: SiteQuality
SIO_000300: 7.79e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.9e-2

QD
type: SiteQuality
SIO_000300: 1.5e1

GenotypeDepth
all individuals: 100
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 73
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 69
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 463
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2325
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 246
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 619
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 206
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1739
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15662
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2952
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 202
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1527
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33100
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 87
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1797
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 515
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 744
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4498
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8782
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56806
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.685385746757588e-5
allele num: 14958
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.235e0

DP
type: SiteQuality
SIO_000300: 1.286757e6

MQRankSum
type: SiteQuality
SIO_000300: 2.85e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

MQ
type: SiteQuality
SIO_000300: 5.955e1

VQSLOD
type: SiteQuality
SIO_000300: -2.154e0

FS
type: SiteQuality
SIO_000300: 1.202e0

QD
type: SiteQuality
SIO_000300: 4.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.74e0

GenotypeDepth
all individuals: 248
bin: 4.25e1
variant carriers: 1

GenotypeDepth
all individuals: 97
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2115
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 398
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2465
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 485
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20509
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1039
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1803
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 265
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 255
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 36
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2713
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2639
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 406
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25828
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 984
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 7
allele frequency: 4.784688995215311e-4
allele num: 14630
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4256
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9438
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.66e0

VQSLOD
type: SiteQuality
SIO_000300: 6.43e-1

QD
type: SiteQuality
SIO_000300: 1.09e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

DP
type: SiteQuality
SIO_000300: 1.19071e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

FS
type: SiteQuality
SIO_000300: 2.702e0

MQ
type: SiteQuality
SIO_000300: 5.946e1

GenotypeDepth
all individuals: 2876
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 101
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 69
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 97
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 398
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2964
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21899
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2788
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23406
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 306
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1123
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2542
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1796
bin: 9.75e1
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European (Finnish)
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East Asian
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African
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European (Non-Finnish)
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South Asian
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allele num: 14532
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Latino
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Other
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QD
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MQ
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ReadPosRankSum
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FS
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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DP
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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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African
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European (Finnish)
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East Asian
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European (Non-Finnish)
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Latino
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Other
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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FS
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ReadPosRankSum
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MQRankSum
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MQ
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InbreedingCoeff
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DP
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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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East Asian
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allele frequency: 2.840909090909091e-4
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African
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European (Non-Finnish)
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European (Finnish)
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South Asian
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Other
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ClippingRankSum
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InbreedingCoeff
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QD
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MQRankSum
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BaseQRankSum
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FS
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DP
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ReadPosRankSum
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MQ
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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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South Asian
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num of homozygotes: 0

Latino
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East Asian
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African
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allele num: 8206
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European (Finnish)
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European (Non-Finnish)
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Other
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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VQSLOD
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MQ
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ReadPosRankSum
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QD
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BaseQRankSum
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DP
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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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num of homozygotes: 0

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

South Asian
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European (Non-Finnish)
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allele num: 66722
num of homozygotes: 0

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

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

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

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

Latino
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Other
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South Asian
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African
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European (Non-Finnish)
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East Asian
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FS
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VQSLOD
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MQRankSum
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QD
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ReadPosRankSum
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BaseQRankSum
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DP
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InbreedingCoeff
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ClippingRankSum
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MQ
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GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 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 frequency: 0.0e0
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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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East Asian
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African
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South Asian
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ReadPosRankSum
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VQSLOD
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MQRankSum
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BaseQRankSum
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FS
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InbreedingCoeff
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QD
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ClippingRankSum
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DP
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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num of homozygotes: 0

East Asian
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Latino
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allele num: 11578
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European (Non-Finnish)
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European (Finnish)
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South Asian
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African
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MQ
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MQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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DP
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ClippingRankSum
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BaseQRankSum
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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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Latino
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African
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East Asian
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European (Finnish)
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South Asian
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Other
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European (Non-Finnish)
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ReadPosRankSum
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DP
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MQ
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BaseQRankSum
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QD
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InbreedingCoeff
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MQRankSum
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FS
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ClippingRankSum
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VQSLOD
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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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African
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Latino
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Other
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East Asian
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European (Non-Finnish)
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South Asian
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FS
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ClippingRankSum
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VQSLOD
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MQRankSum
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QD
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DP
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ReadPosRankSum
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InbreedingCoeff
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MQ
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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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bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.497211728728189e-5
allele num: 66708
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.468e0

ClippingRankSum
type: SiteQuality
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MQ
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SIO_000300: 5.972e1

FS
type: SiteQuality
SIO_000300: 1.609e0

VQSLOD
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SIO_000300: 7.57e-1

DP
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SIO_000300: 2.496893e6

QD
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ReadPosRankSum
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SIO_000300: -9.4e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66700
num of homozygotes: 0

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

Other
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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
allele num: 10402
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
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ClippingRankSum
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SIO_000300: -3.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.29e-1

DP
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SIO_000300: 2.496477e6

InbreedingCoeff
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SIO_000300: 0.0e0

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: 5.25e1
variant carriers: 0

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

South Asian
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allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

Other
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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 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: 8654
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
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SIO_000300: -5.96e-1

ReadPosRankSum
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SIO_000300: 8.67e-1

FS
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ClippingRankSum
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BaseQRankSum
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SIO_000300: -1.429e0

InbreedingCoeff
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SIO_000300: -1.0e-4

VQSLOD
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SIO_000300: 8.699999999999999e-2

QD
type: SiteQuality
SIO_000300: 9.029999999999999e0

DP
type: SiteQuality
SIO_000300: 2.492615e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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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: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16506
num of homozygotes: 0

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

African
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allele count: 1
allele frequency: 9.620935154897056e-5
allele num: 10394
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66656
num of homozygotes: 0

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

ClippingRankSum
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SIO_000300: 1.3e-2

BaseQRankSum
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SIO_000300: 2.74e0

ReadPosRankSum
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SIO_000300: -5.48e-1

MQRankSum
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FS
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SIO_000300: 6.673e0

QD
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VQSLOD
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DP
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InbreedingCoeff
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SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
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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BaseQRankSum
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SIO_000300: 3.0e0

FS
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QD
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DP
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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SIO_000300: -9.52e-1

MQ
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SIO_000300: 6.0e1

ClippingRankSum
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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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bin: 6.25e1
variant carriers: 0

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

Latino
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num of homozygotes: 0

East Asian
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African
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Other
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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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South Asian
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InbreedingCoeff
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VQSLOD
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FS
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MQ
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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DP
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ClippingRankSum
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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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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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African
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Other
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Latino
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European (Finnish)
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European (Non-Finnish)
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DP
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FS
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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QD
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ClippingRankSum
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GenotypeDepth
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

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

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

African
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allele count: 1
allele frequency: 9.632055480639569e-5
allele num: 10382
num of homozygotes: 0

South Asian
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allele count: 90
allele frequency: 5.453884377651194e-3
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66542
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.333e1

VQSLOD
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SIO_000300: 3.54e0

FS
type: SiteQuality
SIO_000300: 7.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.1e-1

ReadPosRankSum
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SIO_000300: 3.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
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SIO_000300: 4.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.39e-1

MQ
type: SiteQuality
SIO_000300: 6.046e1

DP
type: SiteQuality
SIO_000300: 2.469189e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 334
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variant carriers: 0

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

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66528
num of homozygotes: 0

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

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

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

South Asian
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allele frequency: 6.126700159294204e-5
allele num: 16322
num of homozygotes: 0

MQRankSum
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SIO_000300: -1.07e-1

ClippingRankSum
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SIO_000300: -1.49e-1

ReadPosRankSum
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FS
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VQSLOD
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InbreedingCoeff
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DP
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SIO_000300: 2.462836e6

QD
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SIO_000300: 2.737e1

BaseQRankSum
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SIO_000300: -1.667e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.161710037174721e-4
allele num: 8608
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.633911368015414e-5
allele num: 10380
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66478
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.337e0

VQSLOD
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SIO_000300: 7.3e-1

BaseQRankSum
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SIO_000300: 1.87e0

MQRankSum
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SIO_000300: 5.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.76e-1

InbreedingCoeff
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SIO_000300: -4.0e-4

MQ
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SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.452336e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e-2

QD
type: SiteQuality
SIO_000300: 1.383e1

GenotypeDepth
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bin: 9.75e1
variant carriers: 3

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 21

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
all individuals: 2909
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 18
allele frequency: 2.090592334494774e-3
allele num: 8610
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.674531575294934e-5
allele num: 11528
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007699711260828e-5
allele num: 66496
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -8.3e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.829e0

VQSLOD
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SIO_000300: 2.0e0

ClippingRankSum
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SIO_000300: -3.78e-1

ReadPosRankSum
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SIO_000300: 1.71e-1

BaseQRankSum
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SIO_000300: -3.022e0

QD
type: SiteQuality
SIO_000300: 1.266e1

DP
type: SiteQuality
SIO_000300: 2.441855e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 275
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.511006856730422e-5
allele num: 66504
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

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

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

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

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

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

DP
type: SiteQuality
SIO_000300: 2.440377e6

MQRankSum
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SIO_000300: 6.5e-1

ClippingRankSum
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SIO_000300: 1.52e0

FS
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VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.498e1

ReadPosRankSum
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SIO_000300: 3.1e-2

BaseQRankSum
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SIO_000300: 3.18e0

InbreedingCoeff
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SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.934e1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 993
bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 25
allele frequency: 2.40940632228219e-3
allele num: 10376
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.101321585903084e-3
allele num: 908
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66466
num of homozygotes: 0

FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
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BaseQRankSum
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MQ
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QD
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SIO_000300: 1.326e1

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

South Asian
type: Population
allele count: 1
allele frequency: 6.062810719049351e-5
allele num: 16494
num of homozygotes: 0

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

Latino
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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 frequency: 1.504800312998465e-5
allele num: 66454
num of homozygotes: 0

East Asian
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QD
type: SiteQuality
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DP
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FS
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQ
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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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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variant carriers: 1

GenotypeQuality
all individuals: 300
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10364
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66356
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.697164724299878e-5
allele num: 11498
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.172e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.008e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.778e1

MQRankSum
type: SiteQuality
SIO_000300: 1.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 1.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.21e-1

DP
type: SiteQuality
SIO_000300: 2.379903e6

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

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 61
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variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.639097744360903e-4
allele num: 5320
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1098
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7422
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 528
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 362
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.58e-1

VQSLOD
type: SiteQuality
SIO_000300: 8.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.4e-2

DP
type: SiteQuality
SIO_000300: 2.65232e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.7e-1

QD
type: SiteQuality
SIO_000300: 1.156e1

FS
type: SiteQuality
SIO_000300: 2.478e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.739715781600598e-4
allele num: 5348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 376
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 146
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 536
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1108
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7430
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.86e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.571e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.57e-2

FS
type: SiteQuality
SIO_000300: 9.85e-1

QD
type: SiteQuality
SIO_000300: 7.46e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e0

DP
type: SiteQuality
SIO_000300: 2.69733e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.01e0

MQRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 4947
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 382
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7432
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 536
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1112
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

DP
type: SiteQuality
SIO_000300: 2.71165e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.630000000000001e-2

QD
type: SiteQuality
SIO_000300: 7.95e0

VQSLOD
type: SiteQuality
SIO_000300: -4.271e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.27e-1

MQ
type: SiteQuality
SIO_000300: 4.984e1

GenotypeQuality
all individuals: 650
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variant carriers: 0

GenotypeQuality
all individuals: 108
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5680
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 357
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GenotypeQuality
all individuals: 2216
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 7.41839762611276e-4
allele num: 1348
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 68
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5922
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7398
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.05e0

VQSLOD
type: SiteQuality
SIO_000300: -1.402e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.82e-1

MQ
type: SiteQuality
SIO_000300: 5.805e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.6e-2

DP
type: SiteQuality
SIO_000300: 3.20947e5

QD
type: SiteQuality
SIO_000300: 2.63e0

MQRankSum
type: SiteQuality
SIO_000300: -3.82e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.531e0

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 618
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GenotypeQuality
all individuals: 382
bin: 4.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 606
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 2.698327037236913e-4
allele num: 7412
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1370
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 158
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6010
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.933e1

QD
type: SiteQuality
SIO_000300: 1.093e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.45e-2

DP
type: SiteQuality
SIO_000300: 3.25128e5

VQSLOD
type: SiteQuality
SIO_000300: 7.82e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.22e-1

GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 442
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1388
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 82
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6120
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7422
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 154
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.5e-1

DP
type: SiteQuality
SIO_000300: 3.34416e5

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.75e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 4.61e0

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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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
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 frequency: 1.503081316699233e-5
allele num: 66530
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African
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East Asian
type: Population
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Other
type: Population
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MQRankSum
type: SiteQuality
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QD
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
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ReadPosRankSum
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DP
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MQ
type: SiteQuality
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BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -3.59e-1

VQSLOD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.5092439500977e-5
allele num: 66530
num of homozygotes: 0

South Asian
type: Population
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allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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African
type: Population
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allele frequency: 0.0e0
allele num: 10250
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.07e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.416e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.19e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.312e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.59e-1

DP
type: SiteQuality
SIO_000300: 3.306652e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-1

DP
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SIO_000300: 3.309241e6

BaseQRankSum
type: SiteQuality
SIO_000300: 4.61e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e0

VQSLOD
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QD
type: SiteQuality
SIO_000300: 2.024e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.909e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

GenotypeQuality
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bin: 6.25e1
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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bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66544
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16490
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10256
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.934e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.310586e6

FS
type: SiteQuality
SIO_000300: 4.469e0

VQSLOD
type: SiteQuality
SIO_000300: 4.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.9e-2

MQ
type: SiteQuality
SIO_000300: 5.99e1

MQRankSum
type: SiteQuality
SIO_000300: -5.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.56e-1

QD
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SIO_000300: 1.525e1

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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bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66542
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
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: 904
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 6
allele frequency: 3.638127577007034e-4
allele num: 16492
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.312298e6

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.72e0

VQSLOD
type: SiteQuality
SIO_000300: 8.39e-1

FS
type: SiteQuality
SIO_000300: 1.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.0e-1

QD
type: SiteQuality
SIO_000300: 1.513e1

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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variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66546
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.161170459823502e-4
allele num: 8612
num of homozygotes: 0

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.831e1

FS
type: SiteQuality
SIO_000300: 6.138e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 9.01e-1

QD
type: SiteQuality
SIO_000300: 1.183e1

MQRankSum
type: SiteQuality
SIO_000300: 1.82e-1

DP
type: SiteQuality
SIO_000300: 3.313333e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.04e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.334e0

VQSLOD
type: SiteQuality
SIO_000300: -1.943e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16492
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66560
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.42e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.07e-1

FS
type: SiteQuality
SIO_000300: 9.164999999999999e0

DP
type: SiteQuality
SIO_000300: 3.314131e6

QD
type: SiteQuality
SIO_000300: 1.914e1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16144018583043e-4
allele num: 8610
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66574
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.05e0

MQRankSum
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SIO_000300: 1.35e-1

QD
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e0

FS
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DP
type: SiteQuality
SIO_000300: 3.316166e6

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16496
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.731413001167769e-5
allele num: 10276
num of homozygotes: 0

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

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

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

Other
type: Population
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allele num: 904
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.160362032954282e-4
allele num: 8618
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.2e-2

DP
type: SiteQuality
SIO_000300: 3.319774e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.439e0

QD
type: SiteQuality
SIO_000300: 1.112e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.98e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.616e0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.79e-1

GenotypeQuality
all individuals: 2455
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 140
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2360
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2129
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45407
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3346
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1451
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8620
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5008254539997e-5
allele num: 66630
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.69e-1

MQ
type: SiteQuality
SIO_000300: 5.993e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 2.445e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 3.320449e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.735e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.711e0