5-102520439-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102520439
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102520439
    reference: chr 5
allele count: 1
allele frequency: 8.268836409340477e-6
allele num: 120936
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3163A>G
  hgvsp: ENSP00000351126.3:p.Thr1055Ala
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.496A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.707A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3163A>G
  hgvsp: ENSP00000313070.8:p.Thr1055Ala
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.297A>G
  hgvsp: ENSP00000467099.1:p.Thr100Ala
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3163A>G
  hgvsp: ENSP00000416016.1:p.Thr1055Ala
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.811A>G
  hgvsp: ENSP00000424948.1:p.Thr271Ala
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.570A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3590A>G
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9447
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20207
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19605
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3275
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 433
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr1055Ala
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

5-102520442-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102520442
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102520442
    reference: chr 5
allele count: 1
allele frequency: 8.272667107875579e-6
allele num: 120880
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.499G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3166G>T
  hgvsp: ENSP00000351126.3:p.Val1056Leu
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.710G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3166G>T
  hgvsp: ENSP00000313070.8:p.Val1056Leu
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.573G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.814G>T
  hgvsp: ENSP00000424948.1:p.Val272Leu
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3166G>T
  hgvsp: ENSP00000416016.1:p.Val1056Leu
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.300G>T
  hgvsp: ENSP00000467099.1:p.Val101Leu
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3593G>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1074
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 742
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 786
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 488
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Val1056Leu
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

5-102520449-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102520449
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102520449
    reference: chr 5
allele count: 1
allele frequency: 8.279653579294243e-6
allele num: 120778
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.303+4T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3596+4T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3169+4T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3169+4T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+4T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.576+4T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+4T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+4T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3169+4T>C
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19957
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1562
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3255
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9350
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 741
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 784
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: c.3169+4T>C
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

5-102520453-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102520453
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102520453
    reference: chr 5
allele count: 2
allele frequency: 1.657000828500414e-5
allele num: 120700
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3169+8G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.303+8G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3169+8G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3596+8G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.576+8G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+8G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+8G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+8G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3169+8G>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9297
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19339
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1075
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3243
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7170
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3174
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: c.3169+8G>A
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

5-102520455-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102520455
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102520455
    reference: chr 5
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+10G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3169+10G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3169+10G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+10G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3596+10G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.576+10G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+10G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.303+10G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3169+10G>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9279
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1558
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3240
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19682
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1073
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1896
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3168
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD

5-102520465-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102520465
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102520465
    reference: chr 5
allele count: 1
allele frequency: 8.311584686736373e-6
allele num: 120314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3169+20T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.303+20T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3169+20T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3169+20T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.576+20T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+20T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+20T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+20T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3596+20T>C
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2128
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1551
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1869
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1534
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

5-102520478-CCTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102520478
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102520475
    reference: chr 5
allele count: 1
allele frequency: 8.346130733791815e-6
allele num: 119816
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.576+37_576+39delCTT
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3169+37_3169+39delCTT
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+37_817+39delCTT
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3596+37_3596+39delCTT
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.303+37_303+39delCTT
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+37_502+39delCTT
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3169+37_3169+39delCTT
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+37_713+39delCTT
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3169+37_3169+39delCTT
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1513
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16406
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3027
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7697
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2229
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2507
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6720
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 859
  bin: 4.75e1
  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: CCTT
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-102520479-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102520479
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102520479
    reference: chr 5
allele count: 1
allele frequency: 8.345852111500584e-6
allele num: 119820
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3169+34C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3596+34C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+34C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+34C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.576+34C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3169+34C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.303+34C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+34C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3169+34C>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3853
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1512
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5820
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1061
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3003
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 518
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 748
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1799
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2419
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

5-102520489-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102520489
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102520489
    reference: chr 5
allele count: 1
allele frequency: 8.36988181726874e-6
allele num: 119476
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3169+44T>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.576+44T>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+44T>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3169+44T>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+44T>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3596+44T>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+44T>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.303+44T>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3169+44T>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16652
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3935
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13075
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6574
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1273
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9386
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2203
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3619
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2813
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3159
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1678
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

5-102521973-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102521973
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102521973
    reference: chr 5
allele count: 10
allele frequency: 8.570302188855179e-5
allele num: 116682
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3170-48G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3597-48G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1528G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.304-48G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.577-48G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3170-48G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1528G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3170-48G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1528G>C
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9906
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14887
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 652
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12609
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7762
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2815
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5899
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2611
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1398
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 175
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4302
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2626
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum

5-102521986-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102521986
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102521986
    reference: chr 5
allele count: 2
allele frequency: 1.70826286749005e-5
allele num: 117078
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1541C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1541C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3597-35C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.577-35C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3170-35C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.304-35C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3170-35C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3170-35C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1541C>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5647
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2095
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2672
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3447
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19903
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/5-102521986-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102521986
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102521986
    reference: chr 5
allele count: 1
allele frequency: 8.541314337450248e-6
allele num: 117078
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3170-35C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1541C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.577-35C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1541C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3597-35C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1541C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3170-35C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3170-35C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.304-35C>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1843
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5647
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2863
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6828
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10963
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5772
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21340
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 653
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 938
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3456
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1649
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1574
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1451
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

5-102521988-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102521988
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102521988
    reference: chr 5
allele count: 4
allele frequency: 3.417810208999094e-5
allele num: 117034
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.304-33C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3170-33C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1543C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3597-33C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1543C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.577-33C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3170-33C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3170-33C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1543C>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5927
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21952
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2880
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11308
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 617
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1479
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1515
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20602
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

5-102521989-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102521989
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102521989
    reference: chr 5
allele count: 2
allele frequency: 1.707038118161179e-5
allele num: 117162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.304-32G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1544G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.577-32G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3597-32G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3170-32G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3170-32G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1544G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3170-32G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1544G>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22470
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11453
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1790
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6153
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1467
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6273
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2746
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3606
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

5-102521998-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102521998
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102521998
    reference: chr 5
allele count: 1
allele frequency: 8.494300324482272e-6
allele num: 117726
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.304-23G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1553G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3597-23G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3170-23G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.577-23G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1553G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3170-23G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3170-23G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1553G>C
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6437
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2177
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25603
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1689
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 686
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 362
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3877
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3135
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP

5-102522000-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522000
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522000
    reference: chr 5
allele count: 1
allele frequency: 8.481908090043937e-6
allele num: 117898
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.304-21A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1555A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3597-21A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3170-21A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1555A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.577-21A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3170-21A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3170-21A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1555A>G
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25903
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6528
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2931
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 690
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1973
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 582
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1288
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS

5-102522016-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522016
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522016
    reference: chr 5
allele count: 1
allele frequency: 8.380965151946898e-6
allele num: 119318
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1571A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.577-5A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3170-5A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3170-5A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.304-5A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3597-5A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3170-5A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1571A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1571A>G
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 945
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1612
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13807
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 636
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28165
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7303
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28531
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3474
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 3.75e1
  variant carriers: 0
hgvs: c.3170-5A>G
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum

http://identifiers.org/exac.variant/5-102522026-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522026
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522026
    reference: chr 5
allele count: 1
allele frequency: 8.341396683460679e-6
allele num: 119884
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.582C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3175C>A
  hgvsp: ENSP00000313070.8:p.His1059Asn
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1581C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3175C>A
  hgvsp: ENSP00000351126.3:p.His1059Asn
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1581C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.309C>A
  hgvsp: ENSP00000467099.1:p.His104Asn
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3175C>A
  hgvsp: ENSP00000416016.1:p.His1059Asn
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3602C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1581C>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 761
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14433
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 956
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3153
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28060
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1470
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6452
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 5.75e1
  variant carriers: 0
hgvs: p.His1059Asn
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

5-102522029-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522029
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522029
    reference: chr 5
allele count: 1
allele frequency: 8.326949338840222e-6
allele num: 120092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1584T>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1584T>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.585T>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3178T>A
  hgvsp: ENSP00000351126.3:p.Cys1060Ser
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3605T>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1584T>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3178T>A
  hgvsp: ENSP00000416016.1:p.Cys1060Ser
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3178T>A
  hgvsp: ENSP00000313070.8:p.Cys1060Ser
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.312T>A
  hgvsp: ENSP00000467099.1:p.Cys105Ser
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 584
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1649
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3170
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7862
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 962
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27982
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8283
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 47
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 720
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Cys1060Ser
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

5-102522033-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522033
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522033
    reference: chr 5
allele count: 2
allele frequency: 1.663699735471742e-5
allele num: 120214
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3182C>T
  hgvsp: ENSP00000351126.3:p.Ala1061Val
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3609C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.316C>T
  hgvsp: ENSP00000467099.1:p.Ala106Val
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1588C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3182C>T
  hgvsp: ENSP00000416016.1:p.Ala1061Val
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.589C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1588C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3182C>T
  hgvsp: ENSP00000313070.8:p.Ala1061Val
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1588C>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 655
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27814
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14784
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3213
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3556
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3703
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala1061Val
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

5-102522034-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522034
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522034
    reference: chr 5
allele count: 6
allele frequency: 4.987448255224352e-5
allele num: 120302
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.317G>A
  hgvsp: ENST00000511022.1:c.317G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3610G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1589G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3183G>A
  hgvsp: ENST00000358359.3:c.3183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3183G>A
  hgvsp: ENST00000414217.1:c.3183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1589G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.590G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1589G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3183G>A
  hgvsp: ENST00000321521.9:c.3183G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3237
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14815
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8110
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala1061Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

5-102522036-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522036
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522036
    reference: chr 5
allele count: 1
allele frequency: 8.305371914554334e-6
allele num: 120404
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3185G>T
  hgvsp: ENSP00000351126.3:p.Gly1062Val
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3612G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.319G>T
  hgvsp: ENSP00000467099.1:p.Gly107Val
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.592G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1591G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3185G>T
  hgvsp: ENSP00000416016.1:p.Gly1062Val
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1591G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3185G>T
  hgvsp: ENSP00000313070.8:p.Gly1062Val
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1591G>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3252
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1694
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14869
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28558
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1549
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4754
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly1062Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: ReadPosRankSum

5-102522038-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522038
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522038
    reference: chr 5
allele count: 1
allele frequency: 8.300821781356355e-6
allele num: 120470
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3187C>T
  hgvsp: ENST00000414217.1:c.3187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1593C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3614C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3187C>T
  hgvsp: ENST00000358359.3:c.3187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1593C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3187C>T
  hgvsp: ENST00000321521.9:c.3187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1593C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.321C>T
  hgvsp: ENST00000511022.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.594C>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27693
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14933
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8240
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 498
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1565
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 128
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu1063Leu
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

5-102522040-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522040
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522040
    reference: chr 5
allele count: 6
allele frequency: 4.977353043651386e-5
allele num: 120546
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1595G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3189G>A
  hgvsp: ENST00000414217.1:c.3189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1595G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3189G>A
  hgvsp: ENST00000321521.9:c.3189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3189G>A
  hgvsp: ENST00000358359.3:c.3189G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3616G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.323G>A
  hgvsp: ENST00000511022.1:c.323G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.596G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1595G>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14968
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8323
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1580
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 153
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3836
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28584
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1827
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu1063Leu
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum

5-102522051-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522051
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522051
    reference: chr 5
allele count: 2
allele frequency: 1.656342134031205e-5
allele num: 120748
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1606C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.607C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.334C>T
  hgvsp: ENSP00000467099.1:p.Ser112Leu
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3200C>T
  hgvsp: ENSP00000416016.1:p.Ser1067Leu
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3200C>T
  hgvsp: ENSP00000313070.8:p.Ser1067Leu
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1606C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3200C>T
  hgvsp: ENSP00000351126.3:p.Ser1067Leu
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1606C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3627C>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15223
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27467
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8517
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 359
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3904
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser1067Leu
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

5-102522052-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522052
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522052
    reference: chr 5
allele count: 2
allele frequency: 1.656259834042764e-5
allele num: 120754
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.608G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3628G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1607G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3201G>A
  hgvsp: ENST00000321521.9:c.3201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3201G>A
  hgvsp: ENST00000414217.1:c.3201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.335G>A
  hgvsp: ENST00000511022.1:c.335G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3201G>A
  hgvsp: ENST00000358359.3:c.3201G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1607G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1607G>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 290
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1727
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15259
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8543
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3922
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28361
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ser1067Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

5-102522057-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522057
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522057
    reference: chr 5
allele count: 1
allele frequency: 8.272393368849475e-6
allele num: 120884
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3206T>C
  hgvsp: ENSP00000416016.1:p.Leu1069Pro
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3206T>C
  hgvsp: ENSP00000351126.3:p.Leu1069Pro
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3206T>C
  hgvsp: ENSP00000313070.8:p.Leu1069Pro
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1612T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.613T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.340T>C
  hgvsp: ENSP00000467099.1:p.Leu114Pro
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1612T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1612T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3633T>C
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15343
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27390
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3338
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 291
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu1069Pro
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: T
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

5-102522058-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522058
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522058
    reference: chr 5
allele count: 2
allele frequency: 1.654423929587718e-5
allele num: 120888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.341C>T
  hgvsp: ENST00000511022.1:c.341C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3207C>T
  hgvsp: ENST00000321521.9:c.3207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3207C>T
  hgvsp: ENST00000358359.3:c.3207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3634C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.614C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1613C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1613C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3207C>T
  hgvsp: ENST00000414217.1:c.3207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1613C>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1738
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15361
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 233
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 284
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3828
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8617
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Leu1069Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

5-102522059-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522059
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522059
    reference: chr 5
allele count: 2
allele frequency: 1.653931394925738e-5
allele num: 120924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3208G>A
  hgvsp: ENSP00000416016.1:p.Gly1070Arg
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.615G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3635G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1614G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3208G>A
  hgvsp: ENSP00000313070.8:p.Gly1070Arg
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1614G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3208G>A
  hgvsp: ENSP00000351126.3:p.Gly1070Arg
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.342G>A
  hgvsp: ENSP00000467099.1:p.Gly115Arg
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1614G>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15362
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1871
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3963
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly1070Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD

5-102522059-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522059
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522059
    reference: chr 5
allele count: 1
allele frequency: 8.269656974628692e-6
allele num: 120924
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1614G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.615G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3635G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.342G>T
  hgvsp: ENSP00000467099.1:p.Gly115Trp
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3208G>T
  hgvsp: ENSP00000416016.1:p.Gly1070Trp
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3208G>T
  hgvsp: ENSP00000351126.3:p.Gly1070Trp
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1614G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3208G>T
  hgvsp: ENSP00000313070.8:p.Gly1070Trp
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1614G>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1748
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8661
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15362
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27336
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3355
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gly1070Trp
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
reference allele: G
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

5-102522062-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522062
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522062
    reference: chr 5
allele count: 1
allele frequency: 8.264189613566494e-6
allele num: 121004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3211G>A
  hgvsp: ENSP00000351126.3:p.Gly1071Ser
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1617G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.618G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3211G>A
  hgvsp: ENSP00000313070.8:p.Gly1071Ser
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.345G>A
  hgvsp: ENSP00000467099.1:p.Gly116Ser
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1617G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3211G>A
  hgvsp: ENSP00000416016.1:p.Gly1071Ser
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1617G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3638G>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27337
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15383
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8680
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3366
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4969
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Gly1071Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

5-102522068-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522068
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522067
    reference: chr 5
allele count: 1
allele frequency: 8.258047467256841e-6
allele num: 121094
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1624delC
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1624delC
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.352delC
  hgvsp: ENSP00000467099.1:p.Ser118Ter
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3645delC
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1624delC
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3218delC
  hgvsp: ENSP00000351126.3:p.Ser1073Ter
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3218delC
  hgvsp: ENSP00000416016.1:p.Ser1073Ter
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.625delC
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3218delC
  hgvsp: ENSP00000313070.8:p.Ser1073Ter
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 27352
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3373
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8717
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 662
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 526
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15399
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4984
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ser1073Ter
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: TC
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: DP

5-102522073-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522073
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522073
    reference: chr 5
allele count: 3
allele frequency: 2.476228209191759e-5
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1628C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1628C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.629C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3222C>T
  hgvsp: ENST00000321521.9:c.3222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3222C>T
  hgvsp: ENST00000414217.1:c.3222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.356C>T
  hgvsp: ENST00000511022.1:c.356C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1628C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3222C>T
  hgvsp: ENST00000358359.3:c.3222C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3649C>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27318
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8677
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1901
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser1074Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

5-102522074-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522074
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522074
    reference: chr 5
allele count: 1
allele frequency: 8.253276550790664e-6
allele num: 121164
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.357G>A
  hgvsp: ENSP00000467099.1:p.Ala120Thr
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1629G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3650G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3223G>A
  hgvsp: ENSP00000351126.3:p.Ala1075Thr
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1629G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1629G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3223G>A
  hgvsp: ENSP00000416016.1:p.Ala1075Thr
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3223G>A
  hgvsp: ENSP00000313070.8:p.Ala1075Thr
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.630G>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1009
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3388
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15434
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8773
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8674
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala1075Thr
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: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD

5-102522085-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522085
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522085
    reference: chr 5
allele count: 1
allele frequency: 8.247558722618106e-6
allele num: 121248
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.368A>G
  hgvsp: ENST00000511022.1:c.368A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1640A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3234A>G
  hgvsp: ENST00000414217.1:c.3234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3234A>G
  hgvsp: ENST00000321521.9:c.3234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1640A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1640A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3661A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3234A>G
  hgvsp: ENST00000358359.3:c.3234A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.641A>G
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27291
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8797
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8703
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Leu1078Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

5-102522091-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522091
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522091
    reference: chr 5
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3667T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.647T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1646T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.374T>C
  hgvsp: ENST00000511022.1:c.374T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3240T>C
  hgvsp: ENST00000414217.1:c.3240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3240T>C
  hgvsp: ENST00000321521.9:c.3240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1646T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3240T>C
  hgvsp: ENST00000358359.3:c.3240T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1646T>C
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28635
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp1080Asp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

5-102522098-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522098
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522098
    reference: chr 5
allele count: 11
allele frequency: 9.070369576331282e-5
allele num: 121274
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3247C>T
  hgvsp: ENSP00000313070.8:p.Arg1083Cys
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3674C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3247C>T
  hgvsp: ENSP00000351126.3:p.Arg1083Cys
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.654C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3247C>T
  hgvsp: ENSP00000416016.1:p.Arg1083Cys
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1653C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1653C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1653C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.381C>T
  hgvsp: ENSP00000467099.1:p.Arg128Cys
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1771
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8810
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 27276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1010
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3402
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg1083Cys
num of homozygotes: 1
population: Latino
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

5-102522099-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522099
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522099
    reference: chr 5
allele count: 3
allele frequency: 2.473573984597879e-5
allele num: 121282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3248G>A
  hgvsp: ENSP00000351126.3:p.Arg1083His
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3248G>A
  hgvsp: ENSP00000416016.1:p.Arg1083His
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1654G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1654G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1654G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.382G>A
  hgvsp: ENSP00000467099.1:p.Arg128His
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3675G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3248G>A
  hgvsp: ENSP00000313070.8:p.Arg1083His
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.655G>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15471
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27276
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28623
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg1083His
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

5-102522105-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522105
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522105
    reference: chr 5
allele count: 1
allele frequency: 8.244294947896055e-6
allele num: 121296
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1660A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1660A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1660A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3254A>G
  hgvsp: ENSP00000313070.8:p.His1085Arg
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.661A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3254A>G
  hgvsp: ENSP00000416016.1:p.His1085Arg
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3681A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3254A>G
  hgvsp: ENSP00000351126.3:p.His1085Arg
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.388A>G
  hgvsp: ENSP00000467099.1:p.His130Arg
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15470
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His1085Arg
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

5-102522108-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522108
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522108
    reference: chr 5
allele count: 2
allele frequency: 1.648994937585542e-5
allele num: 121286
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3257G>A
  hgvsp: ENSP00000313070.8:p.Arg1086His
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3257G>A
  hgvsp: ENSP00000351126.3:p.Arg1086His
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1663G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3684G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.664G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1663G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.391G>A
  hgvsp: ENSP00000467099.1:p.Arg131His
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3257G>A
  hgvsp: ENSP00000416016.1:p.Arg1086His
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1663G>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1633
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg1086His
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

5-102522108-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522108
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522108
    reference: chr 5
allele count: 1
allele frequency: 8.244974687927709e-6
allele num: 121286
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.391G>T
  hgvsp: ENSP00000467099.1:p.Arg131Leu
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1663G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1663G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3257G>T
  hgvsp: ENSP00000351126.3:p.Arg1086Leu
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3257G>T
  hgvsp: ENSP00000416016.1:p.Arg1086Leu
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1663G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3684G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.664G>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3257G>T
  hgvsp: ENSP00000313070.8:p.Arg1086Leu
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8824
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15467
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8694
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg1086Leu
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: FS

5-102522124-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522124
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522124
    reference: chr 5
allele count: 2
allele frequency: 1.64883180266781e-5
allele num: 121298
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1679T>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3700T>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1679T>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3273T>G
  hgvsp: ENST00000358359.3:c.3273T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1679T>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.407T>G
  hgvsp: ENST00000511022.1:c.407T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3273T>G
  hgvsp: ENST00000321521.9:c.3273T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3273T>G
  hgvsp: ENST00000414217.1:c.3273T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.680T>G
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1019
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8823
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 667
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15444
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27263
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3904
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser1091Ser
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: FS
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

5-102522127-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522127
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522127
    reference: chr 5
allele count: 211
allele frequency: 1.739402832506224e-3
allele num: 121306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1682T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3276T>C
  hgvsp: ENST00000321521.9:c.3276T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.410T>C
  hgvsp: ENST00000511022.1:c.410T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1682T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3276T>C
  hgvsp: ENST00000358359.3:c.3276T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1682T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3276T>C
  hgvsp: ENST00000414217.1:c.3276T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.683T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3703T>C
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 15372
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1775
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3381
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27177
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 8788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 1021
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 308
  bin: 9.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 8.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser1092Ser
num of homozygotes: 2
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

5-102522145-G-GTGCACACA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522145
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522153
    reference: chr 5
allele count: 4
allele frequency: 3.298261816022956e-5
allele num: 121276
alternate allele: GTGCACACA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15315
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27121
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8634
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6802
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 28444
  bin: 6.25e1
  variant carriers: 0
hgvs: c.3289+14_3289+21dupTGCACACA
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum

5-102522147-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522147
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522147
    reference: chr 5
allele count: 2
allele frequency: 1.649457328538911e-5
allele num: 121252
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+7G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+7G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+7G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1702G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+7G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1702G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1702G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+7G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+7G>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15271
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1800
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 2.25e1
  variant carriers: 0
hgvs: c.3289+7G>A
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD

5-102522149-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522149
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522149
    reference: chr 5
allele count: 1
allele frequency: 8.24551856066228e-6
allele num: 121278
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+9A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1704A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+9A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+9A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1704A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+9A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+9A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+9A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1704A>G
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4010
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8619
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.25e1
  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: East Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ

5-102522150-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522150
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522150
    reference: chr 5
allele count: 1
allele frequency: 8.245382585751979e-6
allele num: 121280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1705C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+10C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1705C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+10C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+10C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+10C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1705C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+10C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+10C>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15266
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1797
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27064
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8619
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 116
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28298
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3886
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD

5-102522154-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522154
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522154
    reference: chr 5
allele count: 4
allele frequency: 3.298425002061515e-5
allele num: 121270
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+14T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1709T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+14T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+14T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1709T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+14T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+14T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+14T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1709T>C
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8765
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15258
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 274
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4980
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ

5-102522157-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522157
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522157
    reference: chr 5
allele count: 17
allele frequency: 1.40185374542336e-4
allele num: 121268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+17A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1712A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+17A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+17A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1712A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+17A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1712A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+17A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+17A>G
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8764
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27034
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 538
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15225
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28290
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1629
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

5-102522158-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522158
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522158
    reference: chr 5
allele count: 7
allele frequency: 5.772434153018983e-5
allele num: 121266
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+18C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+18C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+18C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+18C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1713C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1713C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1713C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+18C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+18C>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15189
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1801
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6827
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3881
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8608
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff

5-102522159-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522159
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522159
    reference: chr 5
allele count: 1
allele frequency: 8.246334504312833e-6
allele num: 121266
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+19A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1714A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1714A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+19A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+19A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+19A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1714A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+19A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+19A>G
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8763
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1039
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1914
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28193
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8609
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum

5-102522164-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522164
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522164
    reference: chr 5
allele count: 2
allele frequency: 1.649947201689546e-5
allele num: 121216
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+24G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+24G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1719G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+24G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+24G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+24G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+24G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1719G>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1719G>C
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3420
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15152
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26940
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1803
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 179
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1913
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

5-102522173-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522173
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522173
    reference: chr 5
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1728C>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+33C>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1728C>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+33C>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+33C>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1728C>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+33C>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+33C>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+33C>G
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26802
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15044
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1809
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3414
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1626
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8557
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 178
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: African
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/5-102522175-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522175
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522175
    reference: chr 5
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+35A>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+35A>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+35A>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1730A>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1730A>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+35A>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+35A>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1730A>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+35A>C
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4968
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1913
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
reference allele: A
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

5-102522175-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522175
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522175
    reference: chr 5
allele count: 1
allele frequency: 8.248783304462591e-6
allele num: 121230
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+35A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1730A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+35A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+35A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+35A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1730A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+35A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1730A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+35A>G
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3415
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8718
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26744
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1796
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14964
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27627
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 237
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3874
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

http://identifiers.org/exac.variant/5-102522177-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522177
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522178
    reference: chr 5
allele count: 2
allele frequency: 1.65000165000165e-5
allele num: 121212
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+40dupC
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+40dupC
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1735dupC
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+40dupC
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+40dupC
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1735dupC
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1735dupC
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+40dupC
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+40dupC
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8712
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26747
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1799
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 261
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6825
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 8492
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 159
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP

5-102522182-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522182
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522182
    reference: chr 5
allele count: 1
allele frequency: 8.253549026081216e-6
allele num: 121160
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1737T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+42T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+42T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1737T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1737T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+42T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+42T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+42T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+42T>C
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3422
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14915
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1792
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 285
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 260
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6825
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 27597
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4959
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 233
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP

5-102522184-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522184
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522184
    reference: chr 5
allele count: 2
allele frequency: 1.650818806127839e-5
allele num: 121152
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1739C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+44C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+44C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+44C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+44C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1739C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1739C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+44C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+44C>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8692
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3413
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1798
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14860
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1040
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4955
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8442
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

5-102522192-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522192
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522192
    reference: chr 5
allele count: 2
allele frequency: 1.652155236506022e-5
allele num: 121054
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.423+52C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+52C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+1747C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.696+52C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3716+52C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+52C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3289+52C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+1747C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+1747C>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 683
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26756
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14859
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8683
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 539
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6837
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1923
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/5-102522966-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522966
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522966
    reference: chr 5
allele count: 1
allele frequency: 6.862475981334065e-5
allele num: 14572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+826C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+2521C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+2521C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+826C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.697-49C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+2521C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.424-49C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3290-49C>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3717-49C>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1257
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 717
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 563
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum

5-102522983-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102522983
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102522983
    reference: chr 5
allele count: 1
allele frequency: 6.840881105486387e-5
allele num: 14618
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+843G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.697-32G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+2538G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.424-32G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+2538G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+843G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+2538G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3290-32G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3717-32G>A
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1377
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 634
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2666
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

5-102523016-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102523016
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102523016
    reference: chr 5
allele count: 1
allele frequency: 6.76773145641581e-5
allele num: 14776
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+2571C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+2571C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+876C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.425C>T
  hgvsp: ENST00000511022.1:c.425C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3718C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.698C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+2571C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+876C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3291C>T
  hgvsp: ENST00000358359.3:c.3291C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/29035
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 902
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1261
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1500
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 7.5e0
  variant carriers: 0
hgvs: c.3291C>T
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD

5-102523050-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102523050
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102523050
    reference: chr 5
allele count: 9
allele frequency: 6.045949214026602e-4
allele num: 14886
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+2605A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.732A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+910A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+2605A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+910A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3325A>G
  hgvsp: ENSP00000351126.3:p.Ile1109Val
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.459A>G
  hgvsp: ENSP00000467099.1:p.Ile154Val
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+2605A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3752A>G
  variant of: http://identifiers.org/hgnc/29035
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 917
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1251
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 707
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1492
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 635
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile1109Val
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ

5-102523053-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102523053
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102523053
    reference: chr 5
allele count: 3
allele frequency: 2.013693113169553e-4
allele num: 14898
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+913T>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.735T>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+2608T>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.462T>G
  hgvsp: ENSP00000467099.1:p.Ser155Ala
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3755T>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+2608T>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3328T>G
  hgvsp: ENSP00000351126.3:p.Ser1110Ala
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+913T>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+2608T>G
  variant of: http://identifiers.org/hgnc/29035
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 720
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1259
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2667
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1308
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser1110Ala
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

5-102523118-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102523118
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102523118
    reference: chr 5
allele count: 1
allele frequency: 6.874742197167606e-5
allele num: 14546
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3779+41A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.486+41A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+2673A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+978A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+2673A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.759+41A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+2673A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3352+41A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+978A>G
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1480
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 105
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 630
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

5-102523121-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102523121
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102523121
    reference: chr 5
allele count: 4
allele frequency: 2.758620689655173e-4
allele num: 14500
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.502+2676C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000511724
  gene symbol: PPIP5K2
  hgvsc: ENST00000511724.1:n.759+44C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3352+44C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3779+44C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.817+2676C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3289+981C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3289+981C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.486+44C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.713+2676C>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1256
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 987
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1486
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1172
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 234
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 539
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum

5-102524906-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102524906
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102524906
    reference: chr 5
allele count: 2
allele frequency: 1.862544235425591e-4
allele num: 10738
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3353-1637G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.818-1637G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.714-1637G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3818G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.487-1637G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3290-1637G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.503-1637G>A
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3290-1637G>A
  variant of: http://identifiers.org/hgnc/29035
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 607
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: ClippingRankSum

5-102524939-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102524939
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102524939
    reference: chr 5
allele count: 1
allele frequency: 9.316191540898081e-5
allele num: 10734
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3353-1604T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3290-1604T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3290-1604T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.714-1604T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3839+12T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.818-1604T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.503-1604T>C
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.487-1604T>C
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1597
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 318
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1848
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

5-102524955-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102524955
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102524955
    reference: chr 5
allele count: 1
allele frequency: 9.33184023889511e-5
allele num: 10716
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3290-1588C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.714-1588C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3839+28C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.818-1588C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3290-1588C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.487-1588C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.503-1588C>T
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3353-1588C>T
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1312
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1193
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1631
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1252
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

5-102526496-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 102526496
    reference: chr 5
  end: Position
    type: ExactPosition
    position: 102526496
    reference: chr 5
allele count: 1
allele frequency: 1.024968225984995e-5
allele num: 97564
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000513500
  gene symbol: PPIP5K2
  hgvsc: ENST00000513500.1:n.3840-47A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000313070
  ensembl transcript: ENST00000321521
  gene symbol: PPIP5K2
  hgvsc: ENST00000321521.9:c.3290-47A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000351126
  ensembl transcript: ENST00000358359
  gene symbol: PPIP5K2
  hgvsc: ENST00000358359.3:c.3353-47A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000424948
  ensembl transcript: ENST00000509597
  gene symbol: PPIP5K2
  hgvsc: ENST00000509597.1:c.818-47A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000507966
  gene symbol: PPIP5K2
  hgvsc: ENST00000507966.3:n.714-47A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000416016
  ensembl transcript: ENST00000414217
  gene symbol: PPIP5K2
  hgvsc: ENST00000414217.1:c.3290-47A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl protein: ENSP00000467099
  ensembl transcript: ENST00000511022
  gene symbol: PPIP5K2
  hgvsc: ENST00000511022.1:c.487-47A>G
  variant of: http://identifiers.org/hgnc/29035
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000145725
  ensembl transcript: ENST00000510672
  gene symbol: PPIP5K2
  hgvsc: ENST00000510672.1:n.503-47A>G
  variant of: http://identifiers.org/hgnc/29035
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10780
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1083
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1858
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11296
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 366
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 925
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16387
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 3230
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34974
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 788
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 96
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8141
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66502
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16456
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.061e0

QD
type: SiteQuality
SIO_000300: 9.76e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.6e-1

FS
type: SiteQuality
SIO_000300: 1.421e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.56e-1

DP
type: SiteQuality
SIO_000300: 1.911933e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.99e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.9e-2

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

GenotypeQuality
all individuals: 82
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8588
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.078288353999514e-5
allele num: 16452
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.708e0

DP
type: SiteQuality
SIO_000300: 1.910054e6

FS
type: SiteQuality
SIO_000300: 1.21e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.56e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

VQSLOD
type: SiteQuality
SIO_000300: -2.0e-1

QD
type: SiteQuality
SIO_000300: 8.949999999999999e0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11492
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16436
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505933377507379e-5
allele num: 66404
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.406e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -5.649999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.019e-1

DP
type: SiteQuality
SIO_000300: 1.904707e6

QD
type: SiteQuality
SIO_000300: 1.607e1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34183
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.331545814875262e-4
allele num: 8578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16420
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11490
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66362
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.2394e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.432e0

DP
type: SiteQuality
SIO_000300: 1.900634e6

MQRankSum
type: SiteQuality
SIO_000300: 2.9e0

QD
type: SiteQuality
SIO_000300: 1.102e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.46e0

GenotypeQuality
all individuals: 877
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 146
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16402
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66324
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.166316771635176e-4
allele num: 8574
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.89e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.94e0

MQRankSum
type: SiteQuality
SIO_000300: 1.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.38e-1

DP
type: SiteQuality
SIO_000300: 1.897913e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

FS
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.114e0

QD
type: SiteQuality
SIO_000300: 1.334e1

GenotypeQuality
all individuals: 372
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3107
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512310205069264e-5
allele num: 66124
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.871979e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.53e0

QD
type: SiteQuality
SIO_000300: 1.247e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.599999999999999e-2

GenotypeQuality
all individuals: 1316
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 825
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2414
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 26462
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65870
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.693679720822024e-5
allele num: 10316
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16288
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11394
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -3.295e0

DP
type: SiteQuality
SIO_000300: 1.808586e6

FS
type: SiteQuality
SIO_000300: 3.921e0

VQSLOD
type: SiteQuality
SIO_000300: 1.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

QD
type: SiteQuality
SIO_000300: 1.353e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.03e-1

MQ
type: SiteQuality
SIO_000300: 5.378e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.34e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.58e-1

GenotypeQuality
all individuals: 67
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2221
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 1050
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variant carriers: 0

GenotypeQuality
all individuals: 960
bin: 4.75e1
variant carriers: 0

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65852
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.176193836744295e-4
allele num: 8502
num of homozygotes: 0

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.238e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.5e-1

MQRankSum
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SIO_000300: -2.74e-1

DP
type: SiteQuality
SIO_000300: 1.803382e6

MQ
type: SiteQuality
SIO_000300: 5.901e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.95e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.66e-1

QD
type: SiteQuality
SIO_000300: 2.892e1

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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bin: 2.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16244
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.704968944099378e-5
allele num: 10304
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6550
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65668
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11364
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8452
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.928e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.918e0

ReadPosRankSum
type: SiteQuality
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FS
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.381e0

MQRankSum
type: SiteQuality
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QD
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InbreedingCoeff
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SIO_000300: 2.1e-3

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 3.33e-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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variant carriers: 10

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10810
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15998
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64234
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 9.844457570387872e-4
allele num: 10158
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.489323e6

VQSLOD
type: SiteQuality
SIO_000300: 3.48e0

QD
type: SiteQuality
SIO_000300: 1.254e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.83e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.88e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 6.27e-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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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8398
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6250
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10182
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10906
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.103854987894966e-5
allele num: 64436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16030
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.542082e6

FS
type: SiteQuality
SIO_000300: 5.721e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.98e0

QD
type: SiteQuality
SIO_000300: 8.49e0

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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variant carriers: 1

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64436
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16030
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10906
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6250
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.821253191907288e-5
allele num: 10182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8398
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MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.542082e6

FS
type: SiteQuality
SIO_000300: 5.721e0

QD
type: SiteQuality
SIO_000300: 8.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

VQSLOD
type: SiteQuality
SIO_000300: -8.42e-2

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10174
num of homozygotes: 0

Latino
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allele count: 4
allele frequency: 3.673769287288758e-4
allele num: 10888
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6254
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European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64438
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
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VQSLOD
type: SiteQuality
SIO_000300: -1.913e0

DP
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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SIO_000300: -4.75e-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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variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.101159833777833e-5
allele num: 64492
num of homozygotes: 0

South Asian
type: Population
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allele num: 16054
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
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 876
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6266
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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QD
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ReadPosRankSum
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

VQSLOD
type: SiteQuality
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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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Other
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allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.543352779578356e-5
allele num: 64794
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6316
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11000
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6318
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10234
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.540927021696253e-5
allele num: 64896
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
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VQSLOD
type: SiteQuality
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DP
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.074e0

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6418
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 890
num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16304
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.521606816798539e-5
allele num: 65720
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.671342e6

MQ
type: SiteQuality
SIO_000300: 5.684e1

QD
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MQRankSum
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VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

FS
type: SiteQuality
SIO_000300: 4.419e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.936e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10350
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11246
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.10798924993892e-5
allele num: 16372
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6458
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8546
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66018
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.692418e6

BaseQRankSum
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SIO_000300: -3.923e0

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

Latino
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allele frequency: 0.0e0
allele num: 11272
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66112
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 16412
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.168224299065421e-4
allele num: 8560
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6474
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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VQSLOD
type: SiteQuality
SIO_000300: 6.97e-1

ClippingRankSum
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FS
type: SiteQuality
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DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: -1.942e0

MQ
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MQRankSum
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SIO_000300: -2.18e-1

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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66182
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11282
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.081664098613251e-4
allele num: 6490
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16428
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.6898e1

MQ
type: SiteQuality
SIO_000300: 5.953e1

MQRankSum
type: SiteQuality
SIO_000300: 8.0e-2

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.70416e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.894e0

VQSLOD
type: SiteQuality
SIO_000300: -2.38e0

QD
type: SiteQuality
SIO_000300: 8.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.8e-2

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.05961224859576e-5
allele num: 66228
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16442
num of homozygotes: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

MQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

QD
type: SiteQuality
SIO_000300: 1.338e1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: 0.0e0

DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.5e-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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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.164958061509786e-4
allele num: 8584
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66280
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6512
num of homozygotes: 0

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

East Asian
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South Asian
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allele num: 16456
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Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66308
num of homozygotes: 0

InbreedingCoeff
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BaseQRankSum
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VQSLOD
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FS
type: SiteQuality
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MQRankSum
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QD
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MQ
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DP
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ClippingRankSum
type: SiteQuality
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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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Other
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num of homozygotes: 0

South Asian
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African
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allele frequency: 9.628345850182938e-5
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European (Finnish)
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East Asian
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allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 5
allele frequency: 7.536930961712391e-5
allele num: 66340
num of homozygotes: 0

MQRankSum
type: SiteQuality
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VQSLOD
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QD
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InbreedingCoeff
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ClippingRankSum
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MQ
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ReadPosRankSum
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FS
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DP
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

East Asian
type: Population
allele count: 1
allele frequency: 1.163061177017911e-4
allele num: 8598
num of homozygotes: 0

Other
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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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InbreedingCoeff
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DP
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MQRankSum
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MQ
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FS
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ClippingRankSum
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BaseQRankSum
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ReadPosRankSum
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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East Asian
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Latino
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South Asian
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European (Non-Finnish)
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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QD
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MQRankSum
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ReadPosRankSum
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MQ
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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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South Asian
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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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Other
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DP
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MQRankSum
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QD
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MQ
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InbreedingCoeff
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FS
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ClippingRankSum
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BaseQRankSum
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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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European (Non-Finnish)
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Latino
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African
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Other
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South Asian
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European (Finnish)
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East Asian
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DP
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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QD
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FS
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MQRankSum
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MQ
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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South Asian
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Other
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East Asian
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Latino
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African
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European (Finnish)
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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DP
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VQSLOD
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ClippingRankSum
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MQRankSum
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MQ
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FS
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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East Asian
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European (Non-Finnish)
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South Asian
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Latino
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FS
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QD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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VQSLOD
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DP
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ClippingRankSum
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Non-Finnish)
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European (Finnish)
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Latino
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South Asian
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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FS
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QD
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ReadPosRankSum
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VQSLOD
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ClippingRankSum
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DP
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GenotypeQuality
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African
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Latino
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European (Finnish)
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South Asian
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East Asian
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European (Non-Finnish)
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FS
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MQRankSum
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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QD
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DP
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European (Finnish)
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African
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European (Non-Finnish)
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Latino
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East Asian
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FS
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MQ
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VQSLOD
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DP
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QD
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ClippingRankSum
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SIO_000300: 6.879999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.455e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.03e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 7.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11500
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66638
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.734352e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.02e-1

FS
type: SiteQuality
SIO_000300: 6.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: 3.0e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.051e1

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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bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66674
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11512
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.04e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 2.547e0

QD
type: SiteQuality
SIO_000300: 8.699999999999999e0

MQRankSum
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SIO_000300: 1.62e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.07e-1

DP
type: SiteQuality
SIO_000300: 1.735834e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.29e0

VQSLOD
type: SiteQuality
SIO_000300: 7.000000000000001e-2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8640
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -7.681e-1

MQ
type: SiteQuality
SIO_000300: 5.939e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 3.69e0

DP
type: SiteQuality
SIO_000300: 1.736022e6

MQRankSum
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SIO_000300: -1.478e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.587e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.85e-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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16502
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.499565126113427e-4
allele num: 66686
num of homozygotes: 1

African
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allele count: 1
allele frequency: 9.613535858488752e-5
allele num: 10402
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

DP
type: SiteQuality
SIO_000300: 1.737191e6

BaseQRankSum
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SIO_000300: -1.449e0

FS
type: SiteQuality
SIO_000300: 1.154e0

VQSLOD
type: SiteQuality
SIO_000300: 3.58e0

QD
type: SiteQuality
SIO_000300: 1.419e1

MQ
type: SiteQuality
SIO_000300: 5.951e1

MQRankSum
type: SiteQuality
SIO_000300: 3.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.599999999999999e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10402
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.211827435773146e-4
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.605e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.82e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.781e0

QD
type: SiteQuality
SIO_000300: 1.783e1

ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 6.38e-1

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 3.1e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10400
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66688
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8644
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

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

Other
type: Population
allele count: 0
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allele num: 908
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MQRankSum
type: SiteQuality
SIO_000300: 9.67e-1

DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.3411e1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
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VQSLOD
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QD
type: SiteQuality
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ClippingRankSum
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MQ
type: SiteQuality
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ReadPosRankSum
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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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bin: 1.25e1
variant carriers: 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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allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

European (Finnish)
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allele num: 6610
num of homozygotes: 0

East Asian
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Latino
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allele frequency: 1.732501732501733e-4
allele num: 11544
num of homozygotes: 0

African
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South Asian
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MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQRankSum
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VQSLOD
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ReadPosRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.172e0

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

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

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

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

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

Latino
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allele frequency: 8.662508662508663e-5
allele num: 11544
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Other
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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DP
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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InbreedingCoeff
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MQ
type: SiteQuality
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ClippingRankSum
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FS
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4039
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5018
bin: 7.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66672
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.924187030979411e-4
allele num: 10394
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.82e-1

DP
type: SiteQuality
SIO_000300: 1.737695e6

QD
type: SiteQuality
SIO_000300: 1.039e1

MQRankSum
type: SiteQuality
SIO_000300: 1.84e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.246e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.643e-1

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.25e0

GenotypeQuality
all individuals: 4989
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6882
bin: 9.75e1
variant carriers: 209

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

GenotypeQuality
all individuals: 1907
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1627
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8658
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4025
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3880
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28511
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 203
allele frequency: 1.229706808819966e-2
allele num: 16508
num of homozygotes: 2

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.499625018749062e-5
allele num: 66670
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.64902266043937e-5
allele num: 11562
num of homozygotes: 0

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

African
type: Population
allele count: 1
allele frequency: 9.619084263178146e-5
allele num: 10396
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.786e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-2

DP
type: SiteQuality
SIO_000300: 1.750819e6

VQSLOD
type: SiteQuality
SIO_000300: 4.36e0

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

FS
type: SiteQuality
SIO_000300: 5.24e-1

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

QD
type: SiteQuality
SIO_000300: 1.304e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.2e-2

GenotypeQuality
all individuals: 74
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 52
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3886
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1627
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4987
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variant carriers: 0

GenotypeQuality
all individuals: 4010
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1912
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
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: 10394
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: 2
allele frequency: 3.000570108320581e-5
allele num: 66654
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 6.75e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 5.114e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.74144e6

FS
type: SiteQuality
SIO_000300: 5.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

MQRankSum
type: SiteQuality
SIO_000300: -6.054e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.04e-1

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

GenotypeQuality
all individuals: 22
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8616
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6803
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variant carriers: 2

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1628
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

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

GenotypeQuality
all individuals: 4007
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variant carriers: 0

GenotypeQuality
all individuals: 4986
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variant carriers: 0

GenotypeQuality
all individuals: 28311
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1912
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3888
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 2.75e1
variant carriers: 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: 11552
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001110410852015e-5
allele num: 66642
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.909999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.969e1

VQSLOD
type: SiteQuality
SIO_000300: 1.28e0

MQRankSum
type: SiteQuality
SIO_000300: 7.45e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.78e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.25e0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.740648e6

QD
type: SiteQuality
SIO_000300: 1.117e1

GenotypeQuality
all individuals: 28292
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3887
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4982
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6806
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1630
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1912
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
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: 16508
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.256e1

DP
type: SiteQuality
SIO_000300: 1.740523e6

MQRankSum
type: SiteQuality
SIO_000300: -2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.43e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.934e0

VQSLOD
type: SiteQuality
SIO_000300: 1.13e0

FS
type: SiteQuality
SIO_000300: 4.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.968e1

GenotypeQuality
all individuals: 68
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1912
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6807
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 71
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4982
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1630
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4008
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16508
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.932e1

MQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.042e0

DP
type: SiteQuality
SIO_000300: 1.740455e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.274e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.42e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

GenotypeQuality
all individuals: 21
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 4003
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6810
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 28349
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8622
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3883
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1912
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 2.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.002040693835904e-5
allele num: 66644
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.586e0

DP
type: SiteQuality
SIO_000300: 1.740789e6

QD
type: SiteQuality
SIO_000300: 1.491e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.07e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-3

FS
type: SiteQuality
SIO_000300: 3.281e0

MQRankSum
type: SiteQuality
SIO_000300: -1.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.8e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

GenotypeQuality
all individuals: 8620
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1912
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

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

GenotypeQuality
all individuals: 4986
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4001
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3881
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6824
bin: 9.75e1
variant carriers: 17

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

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.503226387346559e-5
allele num: 66638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10390
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 12
allele frequency: 1.814333232537043e-3
allele num: 6614
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.02e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.37e0

QD
type: SiteQuality
SIO_000300: 1.344e1

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.85e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.42e0

MQ
type: SiteQuality
SIO_000300: 5.943e1

DP
type: SiteQuality
SIO_000300: 1.741245e6

GenotypeQuality
all individuals: 1631
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 88
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3999
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4984
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1914
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28173
bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
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: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66640
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.101851851851852e-4
allele num: 8640
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.974e0

DP
type: SiteQuality
SIO_000300: 1.740645e6

MQRankSum
type: SiteQuality
SIO_000300: 3.91e-1

QD
type: SiteQuality
SIO_000300: 1.187e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.09e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.58e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.3e-3

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4983
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500510173458976e-5
allele num: 66644
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: 10388
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 9.109999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.77e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.580000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.740553e6

MQ
type: SiteQuality
SIO_000300: 5.985e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.65e0

GenotypeQuality
all individuals: 8585
bin: 6.75e1
variant carriers: 0

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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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002191599867904e-5
allele num: 66618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

MQ
type: SiteQuality
SIO_000300: 5.95e1

MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.73e-1

DP
type: SiteQuality
SIO_000300: 1.740186e6

QD
type: SiteQuality
SIO_000300: 1.366e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.19e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.39e-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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501366243281386e-5
allele num: 66606
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.661e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.737897e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -6.45e-1

FS
type: SiteQuality
SIO_000300: 8.827e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.93e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.7e-1

QD
type: SiteQuality
SIO_000300: 1.166e1

GenotypeQuality
all individuals: 1627
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 27627
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501140867058965e-5
allele num: 66616
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

DP
type: SiteQuality
SIO_000300: 1.736026e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.505e0

FS
type: SiteQuality
SIO_000300: 1.4649e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.02e0

MQ
type: SiteQuality
SIO_000300: 5.893e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.12e0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 103
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3981
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1913
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.63020030816641e-5
allele num: 10384
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.4649e1

VQSLOD
type: SiteQuality
SIO_000300: -1.505e0

MQRankSum
type: SiteQuality
SIO_000300: 2.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.12e0

MQ
type: SiteQuality
SIO_000300: 5.893e1

DP
type: SiteQuality
SIO_000300: 1.736026e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.33e-1

QD
type: SiteQuality
SIO_000300: 9.630000000000001e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4964
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.315886984715146e-4
allele num: 8636
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.198e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-3

QD
type: SiteQuality
SIO_000300: 1.236e1

DP
type: SiteQuality
SIO_000300: 1.736149e6

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 154
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10382
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11544
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66596
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.46e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -5.054999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e0

MQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.697e0

FS
type: SiteQuality
SIO_000300: 1.959e0

DP
type: SiteQuality
SIO_000300: 1.735376e6

GenotypeQuality
all individuals: 173
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
all individuals: 277
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3969
bin: 7.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003273568189326e-5
allele num: 66594
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

FS
type: SiteQuality
SIO_000300: 6.568e0

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.162e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.426e0

DP
type: SiteQuality
SIO_000300: 1.73507e6

GenotypeQuality
all individuals: 335
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3857
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GenotypeQuality
all individuals: 4941
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10368
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005168890491646e-5
allele num: 66552
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -8.64e-1

DP
type: SiteQuality
SIO_000300: 1.735877e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.55e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.58e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.06e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.18e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1600
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4192
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.639344262295082e-3
allele num: 610
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.8e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.666e0

DP
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SIO_000300: 3.07248e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.19e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.868e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.51e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.122e1

MQRankSum
type: SiteQuality
SIO_000300: 1.45e0

GenotypeQuality
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bin: 2.5e0
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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variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1600
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7614
num of homozygotes: 0

African
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allele count: 1
allele frequency: 1.644736842105263e-3
allele num: 608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.350000000000001e-1

DP
type: SiteQuality
SIO_000300: 3.09183e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.37e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.73e-2

QD
type: SiteQuality
SIO_000300: 1.168e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.47e-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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bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1602
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4344
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.312335958005249e-4
allele num: 7620
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.0e-2

FS
type: SiteQuality
SIO_000300: 9.04e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 3.12259e5

MQRankSum
type: SiteQuality
SIO_000300: 5.32e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.32e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.917e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.416e1

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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variant carriers: 9

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 662
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 198
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.130710085933967e-3
allele num: 4422
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 2.4906600249066e-3
allele num: 1606
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.84e0

FS
type: SiteQuality
SIO_000300: 1.755e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.51e-2

DP
type: SiteQuality
SIO_000300: 3.13597e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.17e-1

QD
type: SiteQuality
SIO_000300: 1.406e1

VQSLOD
type: SiteQuality
SIO_000300: 2.29e0

MQRankSum
type: SiteQuality
SIO_000300: 5.659999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

GenotypeQuality
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bin: 4.25e1
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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4428
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 190
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1608
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 3.937007874015748e-4
allele num: 7620
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -5.41e-1

DP
type: SiteQuality
SIO_000300: 3.13298e5

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 2.08e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.33e-2

FS
type: SiteQuality
SIO_000300: 2.239e0

MQ
type: SiteQuality
SIO_000300: 5.953e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.43e-1

QD
type: SiteQuality
SIO_000300: 9.1e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.5e0
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 596
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4174
num of homozygotes: 0

South Asian
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allele frequency: 1.314060446780552e-4
allele num: 7610
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 200
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Other
type: Population
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allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.5e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
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MQRankSum
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ClippingRankSum
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VQSLOD
type: SiteQuality
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DP
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InbreedingCoeff
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SIO_000300: -1.81e-2

ReadPosRankSum
type: SiteQuality
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QD
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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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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4138
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

Latino
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allele frequency: 5.319148936170213e-3
allele num: 188
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 1592
num of homozygotes: 0

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

South Asian
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allele frequency: 3.942181340341655e-4
allele num: 7610
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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FS
type: SiteQuality
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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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bin: 9.75e1
variant carriers: 2

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

Other
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African
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7502
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 7.390983000739098e-4
allele num: 2706
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.952e-1

InbreedingCoeff
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MQ
type: SiteQuality
SIO_000300: 5.974e1

BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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DP
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FS
type: SiteQuality
SIO_000300: 2.308e0

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e-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
all individuals: 470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 801
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 7.575757575757576e-3
allele num: 132
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7500
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2704
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.61816e5

ClippingRankSum
type: SiteQuality
SIO_000300: 2.3e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.98e0

QD
type: SiteQuality
SIO_000300: 1.466e1

MQ
type: SiteQuality
SIO_000300: 5.933e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.53e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.3e-1

GenotypeQuality
all individuals: 318
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 606
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1750
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 186
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: NaN
allele num: 0
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.334400854016547e-4
allele num: 7494
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2694
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.24e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.136e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.68e-2

FS
type: SiteQuality
SIO_000300: 3.881e0

MQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.76e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.15e-1

QD
type: SiteQuality
SIO_000300: 1.35e1

DP
type: SiteQuality
SIO_000300: 1.6119e5