11-68343509-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68343509
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68343509
    reference: chr 11
allele count: 1
allele frequency: 8.256002113536541e-6
allele num: 121124
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1543C>G
  hgvsp: ENSP00000265637.4:p.Leu515Val
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.751C>G
  hgvsp: ENSP00000436209.1:p.Leu251Val
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1543C>G
  hgvsp: ENSP00000377389.2:p.Leu515Val
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.206C>G
  hgvsp: ENSP00000434426.1:p.Leu70Val
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1543C>G
  hgvsp: ENSP00000377388.2:p.Leu515Val
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1390C>G
  hgvsp: ENSP00000265636.4:p.Leu464Val
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1390C>G
  hgvsp: ENSP00000437329.1:p.Leu464Val
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1543C>G
  hgvsp: ENSP00000433058.1:p.Leu515Val
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1543C>G
  hgvsp: ENSP00000377390.3:p.Leu515Val
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.847C>G
  hgvsp: ENSP00000434429.1:p.Leu283Val
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1543C>G
  hgvsp: ENSP00000431415.1:p.Leu515Val
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1543C>G
  hgvsp: ENSP00000433565.1:p.Leu515Val
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10913
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12240
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu515Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

11-68343515-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68343515
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68343515
    reference: chr 11
allele count: 1
allele frequency: 8.273351534706709e-6
allele num: 120870
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1545+4G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1545+4G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1545+4G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.849+4G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.753+4G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1545+4G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.208+4G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1545+4G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1392+4G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1545+4G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1392+4G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1545+4G>A
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2068
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7226
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1545+4G>A
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff

11-68343515-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68343515
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68343515
    reference: chr 11
allele count: 1
allele frequency: 8.273351534706709e-6
allele num: 120870
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.753+4G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1545+4G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.208+4G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.849+4G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1545+4G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1545+4G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1545+4G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1545+4G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1545+4G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1545+4G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1392+4G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1392+4G>T
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11675
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1545+4G>T
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP

11-68343526-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68343526
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68343526
    reference: chr 11
allele count: 2
allele frequency: 1.657275439177991e-5
allele num: 120680
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1545+15G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1545+15G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.849+15G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.208+15G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1545+15G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.753+15G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1545+15G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1545+15G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1392+15G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1392+15G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1545+15G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1545+15G>A
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7211
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1078
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10835
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11219
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

11-68343533-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68343533
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68343533
    reference: chr 11
allele count: 2
allele frequency: 1.660302174995849e-5
allele num: 120460
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1545+22T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1545+22T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1545+22T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.753+22T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1545+22T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1545+22T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.208+22T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1545+22T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1392+22T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1392+22T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.849+22T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1545+22T>G
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1984
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13499
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3124
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4693
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7204
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

11-68343535-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68343535
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68343535
    reference: chr 11
allele count: 1
allele frequency: 8.30357884248111e-6
allele num: 120430
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1545+24T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.753+24T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1545+24T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1545+24T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.849+24T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1392+24T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1392+24T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1545+24T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.208+24T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1545+24T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1545+24T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1545+24T>G
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9830
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 449
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2085
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2066
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

11-68343543-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68343543
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68343543
    reference: chr 11
allele count: 2
allele frequency: 1.663921196692125e-5
allele num: 120198
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1545+32T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1545+32T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1545+32T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.849+32T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1392+32T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1392+32T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.208+32T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1545+32T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1545+32T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1545+32T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.753+32T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1545+32T>A
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 582
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2643
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8118
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4689
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2067
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12728
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1023
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7191
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

11-68350477-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68350477
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68350477
    reference: chr 11
allele count: 2
allele frequency: 9.256687957048968e-5
allele num: 21606
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1546-34T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1546-34T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-4969T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.850-34T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1546-34T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-4936T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-4918T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.209-34T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-4918T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-4918T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-4918T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1546-34T>C
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1623
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1697
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1207
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3491
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD

11-68350478-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68350478
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68350478
    reference: chr 11
allele count: 2
allele frequency: 9.255831173639393e-5
allele num: 21608
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-4917G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.209-33G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-4968G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1546-33G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1546-33G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-4917G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-4917G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-4935G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1546-33G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1546-33G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.850-33G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-4917G>A
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1203
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

11-68350488-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68350488
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68350488
    reference: chr 11
allele count: 1
allele frequency: 4.623208506703652e-5
allele num: 21630
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-4907C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.850-23C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-4907C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1546-23C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-4907C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.209-23C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-4907C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-4958C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1546-23C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1546-23C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1546-23C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-4925C>G
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 473
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 561
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

11-68350505-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68350505
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68350505
    reference: chr 11
allele count: 59
allele frequency: 2.711646291019395e-3
allele num: 21758
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.209-6A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1546-6A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1546-6A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-4941A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1546-6A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-4890A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-4890A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.850-6A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1546-6A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-4890A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-4908A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-4890A>G
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 385
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 947
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 3.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: c.1546-6A>G
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

11-68350581-ATTC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68350581
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68350578
    reference: chr 11
allele count: 1
allele frequency: 4.513450081242101e-5
allele num: 22156
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1622_1624delCTT
  hgvsp: ENSP00000377389.2:p.Ser541del
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1622_1624delCTT
  hgvsp: ENSP00000377388.2:p.Ser541del
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-4808_754-4806delCTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-4826_1546-4824delCTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-4808_1393-4806delCTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-4859_1546-4857delCTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.926_928delCTT
  hgvsp: ENSP00000434429.1:p.Ser309del
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1622_1624delCTT
  hgvsp: ENSP00000377390.3:p.Ser541del
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.285_287delCTT
  hgvsp: ENSP00000434426.1:p.Ser96del
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-4808_1393-4806delCTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-4808_1546-4806delCTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1622_1624delCTT
  hgvsp: ENSP00000433058.1:p.Ser541del
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1888
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 745
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3658
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1724
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser541del
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: ATTC
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

11-68350597-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68350597
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68350597
    reference: chr 11
allele count: 1
allele frequency: 4.533091568449683e-5
allele num: 22060
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1632A>G
  hgvsp: ENST00000393799.2:c.1632A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-4816A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1632A>G
  hgvsp: ENST00000393801.3:c.1632A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.936A>G
  hgvsp: ENST00000534534.1:c.936A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-4798A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1632A>G
  hgvsp: ENST00000524904.1:c.1632A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-4798A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.295A>G
  hgvsp: ENST00000525421.1:c.295A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-4849A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-4798A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1632A>G
  hgvsp: ENST00000393800.2:c.1632A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-4798A>G
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1765
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 616
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3631
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1632A>G
num of homozygotes: 0
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

11-68350600-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68350600
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68350600
    reference: chr 11
allele count: 1
allele frequency: 4.536381781890764e-5
allele num: 22044
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1632+3G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.936+3G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.295+3G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-4795G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1632+3G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-4795G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1632+3G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-4795G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-4813G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1632+3G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-4846G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-4795G>A
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 813
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1736
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3616
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1632+3G>A
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP

11-68350607-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68350607
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68350607
    reference: chr 11
allele count: 1
allele frequency: 4.557054320087495e-5
allele num: 21944
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-4788G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.936+10G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.295+10G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-4839G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-4788G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1632+10G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1632+10G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-4788G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-4788G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-4806G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1632+10G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1632+10G>T
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 906
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3535
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 568
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

11-68350639-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68350639
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68350639
    reference: chr 11
allele count: 1
allele frequency: 4.699689820471849e-5
allele num: 21278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-4756A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-4756A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-4807A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.936+42A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1632+42A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1632+42A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.295+42A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-4756A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-4756A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1632+42A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-4774A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1632+42A>T
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2009
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 569
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 203
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 637
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1269
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: East Asian
population: Other
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS

11-68355216-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355216
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355216
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 17100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-179G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-179G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-179G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-179G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-179G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-230G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-197G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-179G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-179G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1473G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-197G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-179G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.296-50G>A
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14551
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1200
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31948
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4024
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2435
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD

11-68355235-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355235
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355235
    reference: chr 11
allele count: 1
allele frequency: 5.491488193300384e-5
allele num: 18210
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-160T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.296-31T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-160T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-178T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-160T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-178T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1492T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-160T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-160T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-160T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-160T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-211T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-160T>C
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3540
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28518
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19388
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-68355249-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355249
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355249
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 21690
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-164T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-164T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-197T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.296-17T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-146T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-146T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-146T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-146T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-146T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-146T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-146T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1506T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-146T>C
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28247
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19634
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3022
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: East Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

11-68355290-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355290
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355290
    reference: chr 11
allele count: 1
allele frequency: 1.388079176036201e-5
allele num: 72042
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-105C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1547C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-123C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-105C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-105C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-123C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-105C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-105C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.320C>T
  hgvsp: ENST00000525421.1:c.320C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-105C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-105C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-105C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-156C>T
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3318
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27771
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22858
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu108Leu
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum

11-68355292-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355292
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355292
    reference: chr 11
allele count: 121
allele frequency: 1.589052609460773e-3
allele num: 76146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1549A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-121A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-103A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-103A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.322A>G
  hgvsp: ENST00000525421.1:c.322A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-103A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-103A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-103A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-103A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-121A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-154A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-103A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-103A>G
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 3.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 1.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1201
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2739
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21214
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 29457
  bin: 2.25e1
  variant carriers: 29
genotype quality: GenotypeQuality
hgvs: p.Leu108Leu
num of homozygotes: 1
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/11-68355298-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355298
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355298
    reference: chr 11
allele count: 2
allele frequency: 2.282688093498904e-5
allele num: 87616
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-115A>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-97A>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1555A>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.328A>C
  hgvsp: ENST00000525421.1:c.328A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-97A>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-97A>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-97A>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-97A>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-97A>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-148A>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-115A>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-97A>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-97A>C
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34676
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16015
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu110Leu
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS

11-68355298-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355298
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355298
    reference: chr 11
allele count: 58
allele frequency: 6.619795471146823e-4
allele num: 87616
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-97A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.328A>G
  hgvsp: ENST00000525421.1:c.328A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-115A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-97A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-97A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-97A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-148A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-97A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1555A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-97A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-115A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-97A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-97A>G
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1262
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1031
  bin: 1.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 4372
  bin: 2.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16015
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 34676
  bin: 2.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2263
  bin: 1.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu110Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

11-68355303-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355303
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355303
    reference: chr 11
allele count: 1
allele frequency: 1.055520371543171e-5
allele num: 94740
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-92A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-92A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-92A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-143A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-92A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-110A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1560A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-92A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.333A>G
  hgvsp: ENSP00000434426.1:p.Lys112Arg
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-92A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-92A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-92A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-110A>G
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12702
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37871
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4979
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys112Arg
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: QD

11-68355327-AT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355327
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355326
    reference: chr 11
allele count: 1
allele frequency: 8.566337719298245e-6
allele num: 116736
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-85delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-67delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*21delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-67delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-67delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-67delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1585delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-85delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-67delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-67delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-118delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-67delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-67delT
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: 3' UTR
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46553
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7666
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2293
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: AT
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

11-68355345-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355345
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355345
    reference: chr 11
allele count: 1
allele frequency: 8.286514526259965e-6
allele num: 120678
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-50G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-101G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-50G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-50G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-68G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1602G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-50G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-50G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-50G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-50G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*38G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-68G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-50G>A
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

11-68355345-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355345
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355345
    reference: chr 11
allele count: 7
allele frequency: 5.800560168381975e-5
allele num: 120678
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-101G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-68G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-50G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-50G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*38G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-50G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-68G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-50G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-50G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-50G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-50G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-50G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1602G>T
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47126
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8641
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3591
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

11-68355355-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355355
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355355
    reference: chr 11
allele count: 1
allele frequency: 8.250961236984109e-6
allele num: 121198
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-40A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-40A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-40A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1612A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*48A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-40A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-58A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-58A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-40A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-40A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-91A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-40A>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-40A>T
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8822
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47196
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

11-68355361-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355361
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355361
    reference: chr 11
allele count: 1
allele frequency: 8.245110649384915e-6
allele num: 121284
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*54A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-34A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-52A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-34A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-85A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1618A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-34A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-52A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-34A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-34A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-34A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-34A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-34A>G
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8881
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum

11-68355366-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355366
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355366
    reference: chr 11
allele count: 2
allele frequency: 1.648532805802836e-5
allele num: 121320
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-47A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-29A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-29A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-29A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-29A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-47A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-29A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*59A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-29A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-80A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1623A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-29A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-29A>G
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 484
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8899
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

11-68355374-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355374
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355374
    reference: chr 11
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-39C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-21C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1631C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*67C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-21C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-39C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-21C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-21C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-21C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-21C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-72C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-21C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-21C>T
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8911
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47178
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP

11-68355378-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355378
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355378
    reference: chr 11
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-17G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-17G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*71G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-35G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-17G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-17G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-17G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-17G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-35G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-68G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1635G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-17G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-17G>C
  variant of: http://identifiers.org/hgnc/1173
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3733
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8932
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

11-68355394-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355394
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355394
    reference: chr 11
allele count: 1
allele frequency: 8.236825198095647e-6
allele num: 121406
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*87G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1633-1G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.754-1G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.937-1G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-52G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1546-1G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1651G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1633-1G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1393-1G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1633-1G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_acceptor_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1393-1G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1633-19G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1546-19G>C
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: splice acceptor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8949
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1633-1G>C
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: G
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: QD

11-68355421-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355421
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355421
    reference: chr 11
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1419A>G
  hgvsp: ENST00000529710.1:c.1419A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.780A>G
  hgvsp: ENST00000534190.1:c.780A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*114A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.963A>G
  hgvsp: ENST00000534534.1:c.963A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1659A>G
  hgvsp: ENST00000393799.2:c.1659A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1659A>G
  hgvsp: ENST00000393800.2:c.1659A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1554A>G
  hgvsp: ENST00000527403.2:c.1554A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1641A>G
  hgvsp: ENST00000524904.1:c.1641A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1572A>G
  hgvsp: ENST00000524845.1:c.1572A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1419A>G
  hgvsp: ENST00000265636.5:c.1419A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1659A>G
  hgvsp: ENST00000393801.3:c.1659A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-25A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1678A>G
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8956
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln553Gln
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

11-68355427-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355427
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355427
    reference: chr 11
allele count: 2
allele frequency: 1.647310765175851e-5
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1425G>A
  hgvsp: ENST00000265636.5:c.1425G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1665G>A
  hgvsp: ENST00000393800.2:c.1665G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1647G>A
  hgvsp: ENST00000524904.1:c.1647G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-19G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.786G>A
  hgvsp: ENST00000534190.1:c.786G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1665G>A
  hgvsp: ENST00000393799.2:c.1665G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1684G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1665G>A
  hgvsp: ENST00000393801.3:c.1665G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1578G>A
  hgvsp: ENST00000524845.1:c.1578G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1560G>A
  hgvsp: ENST00000527403.2:c.1560G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.969G>A
  hgvsp: ENST00000534534.1:c.969G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*120G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1425G>A
  hgvsp: ENST00000529710.1:c.1425G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47170
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8954
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr555Thr
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/11-68355441-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355441
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355441
    reference: chr 11
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*134A>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1679A>C
  hgvsp: ENSP00000377388.2:p.Asp560Ala
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1574A>C
  hgvsp: ENSP00000433565.1:p.Asp525Ala
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1661A>C
  hgvsp: ENSP00000433058.1:p.Asp554Ala
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.800A>C
  hgvsp: ENSP00000436209.1:p.Asp267Ala
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1546-5A>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1439A>C
  hgvsp: ENSP00000265636.4:p.Asp480Ala
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1439A>C
  hgvsp: ENSP00000437329.1:p.Asp480Ala
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.983A>C
  hgvsp: ENSP00000434429.1:p.Asp328Ala
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1698A>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1679A>C
  hgvsp: ENSP00000377389.2:p.Asp560Ala
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1592A>C
  hgvsp: ENSP00000431415.1:p.Asp531Ala
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1679A>C
  hgvsp: ENSP00000377390.3:p.Asp560Ala
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp560Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

11-68355456-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355456
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355456
    reference: chr 11
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1556A>G
  hgvsp: ENSP00000265637.4:p.Asn519Ser
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1454A>G
  hgvsp: ENSP00000437329.1:p.Asn485Ser
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1694A>G
  hgvsp: ENSP00000377389.2:p.Asn565Ser
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.998A>G
  hgvsp: ENSP00000434429.1:p.Asn333Ser
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1694A>G
  hgvsp: ENSP00000377388.2:p.Asn565Ser
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1676A>G
  hgvsp: ENSP00000433058.1:p.Asn559Ser
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1694A>G
  hgvsp: ENSP00000377390.3:p.Asn565Ser
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1607A>G
  hgvsp: ENSP00000431415.1:p.Asn536Ser
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1454A>G
  hgvsp: ENSP00000265636.4:p.Asn485Ser
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1589A>G
  hgvsp: ENSP00000433565.1:p.Asn530Ser
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*149A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.815A>G
  hgvsp: ENSP00000436209.1:p.Asn272Ser
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1713A>G
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47168
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn565Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: ClippingRankSum

11-68355457-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355457
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355457
    reference: chr 11
allele count: 4
allele frequency: 3.294621530351701e-5
allele num: 121410
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1695C>T
  hgvsp: ENST00000393800.2:c.1695C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1714C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1608C>T
  hgvsp: ENST00000524845.1:c.1608C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1590C>T
  hgvsp: ENST00000527403.2:c.1590C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*150C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1455C>T
  hgvsp: ENST00000529710.1:c.1455C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1695C>T
  hgvsp: ENST00000393801.3:c.1695C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.816C>T
  hgvsp: ENST00000534190.1:c.816C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1557C>T
  hgvsp: ENST00000265637.4:c.1557C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1677C>T
  hgvsp: ENST00000524904.1:c.1677C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1695C>T
  hgvsp: ENST00000393799.2:c.1695C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.999C>T
  hgvsp: ENST00000534534.1:c.999C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1455C>T
  hgvsp: ENST00000265636.5:c.1455C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 494
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn565Asn
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum

11-68355458-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355458
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355458
    reference: chr 11
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1678G>A
  hgvsp: ENSP00000433058.1:p.Asp560Asn
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1456G>A
  hgvsp: ENSP00000265636.4:p.Asp486Asn
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1456G>A
  hgvsp: ENSP00000437329.1:p.Asp486Asn
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1715G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1696G>A
  hgvsp: ENSP00000377389.2:p.Asp566Asn
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.817G>A
  hgvsp: ENSP00000436209.1:p.Asp273Asn
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1696G>A
  hgvsp: ENSP00000377388.2:p.Asp566Asn
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1591G>A
  hgvsp: ENSP00000433565.1:p.Asp531Asn
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1609G>A
  hgvsp: ENSP00000431415.1:p.Asp537Asn
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1558G>A
  hgvsp: ENSP00000265637.4:p.Asp520Asn
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1696G>A
  hgvsp: ENSP00000377390.3:p.Asp566Asn
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1000G>A
  hgvsp: ENSP00000434429.1:p.Asp334Asn
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*151G>A
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp566Asn
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

11-68355469-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355469
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355469
    reference: chr 11
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1467T>G
  hgvsp: ENSP00000265636.4:p.Phe489Leu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*162T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1689T>G
  hgvsp: ENSP00000433058.1:p.Phe563Leu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1011T>G
  hgvsp: ENSP00000434429.1:p.Phe337Leu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1467T>G
  hgvsp: ENSP00000437329.1:p.Phe489Leu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1707T>G
  hgvsp: ENSP00000377389.2:p.Phe569Leu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1602T>G
  hgvsp: ENSP00000433565.1:p.Phe534Leu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1707T>G
  hgvsp: ENSP00000377388.2:p.Phe569Leu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1569T>G
  hgvsp: ENSP00000265637.4:p.Phe523Leu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1620T>G
  hgvsp: ENSP00000431415.1:p.Phe540Leu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.828T>G
  hgvsp: ENSP00000436209.1:p.Phe276Leu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1726T>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1707T>G
  hgvsp: ENSP00000377390.3:p.Phe569Leu
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47164
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe569Leu
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

11-68355476-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355476
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355476
    reference: chr 11
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1627C>G
  hgvsp: ENSP00000431415.1:p.Gln543Glu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1609C>G
  hgvsp: ENSP00000433565.1:p.Gln537Glu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1576C>G
  hgvsp: ENSP00000265637.4:p.Gln526Glu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1474C>G
  hgvsp: ENSP00000437329.1:p.Gln492Glu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*169C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1018C>G
  hgvsp: ENSP00000434429.1:p.Gln340Glu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1714C>G
  hgvsp: ENSP00000377389.2:p.Gln572Glu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1696C>G
  hgvsp: ENSP00000433058.1:p.Gln566Glu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1714C>G
  hgvsp: ENSP00000377388.2:p.Gln572Glu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.835C>G
  hgvsp: ENSP00000436209.1:p.Gln279Glu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1714C>G
  hgvsp: ENSP00000377390.3:p.Gln572Glu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1474C>G
  hgvsp: ENSP00000265636.4:p.Gln492Glu
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1733C>G
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47159
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln572Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

11-68355478-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355478
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355478
    reference: chr 11
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*171A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1735A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1716A>G
  hgvsp: ENST00000393800.2:c.1716A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1476A>G
  hgvsp: ENST00000265636.5:c.1476A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1698A>G
  hgvsp: ENST00000524904.1:c.1698A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1716A>G
  hgvsp: ENST00000393799.2:c.1716A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1578A>G
  hgvsp: ENST00000265637.4:c.1578A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1476A>G
  hgvsp: ENST00000529710.1:c.1476A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1629A>G
  hgvsp: ENST00000524845.1:c.1629A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1611A>G
  hgvsp: ENST00000527403.2:c.1611A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1716A>G
  hgvsp: ENST00000393801.3:c.1716A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.837A>G
  hgvsp: ENST00000534190.1:c.837A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1020A>G
  hgvsp: ENST00000534534.1:c.1020A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3743
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47158
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8955
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln572Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

11-68355486-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355486
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355486
    reference: chr 11
allele count: 1
allele frequency: 8.236553825879253e-6
allele num: 121410
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1706T>C
  hgvsp: ENSP00000433058.1:p.Ile569Thr
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1743T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1586T>C
  hgvsp: ENSP00000265637.4:p.Ile529Thr
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1484T>C
  hgvsp: ENSP00000265636.4:p.Ile495Thr
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1028T>C
  hgvsp: ENSP00000434429.1:p.Ile343Thr
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1724T>C
  hgvsp: ENSP00000377388.2:p.Ile575Thr
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*179T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1484T>C
  hgvsp: ENSP00000437329.1:p.Ile495Thr
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1619T>C
  hgvsp: ENSP00000433565.1:p.Ile540Thr
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1637T>C
  hgvsp: ENSP00000431415.1:p.Ile546Thr
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1724T>C
  hgvsp: ENSP00000377390.3:p.Ile575Thr
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.845T>C
  hgvsp: ENSP00000436209.1:p.Ile282Thr
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1724T>C
  hgvsp: ENSP00000377389.2:p.Ile575Thr
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47150
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3742
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile575Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

11-68355506-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355506
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355506
    reference: chr 11
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1490+14T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1034+14T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.851+14T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1625+14T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1712+14T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1749+14T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1592+14T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1490+14T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*185+14T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1730+14T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1730+14T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1643+14T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1730+14T>C
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47086
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8946
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff

11-68355514-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355514
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355514
    reference: chr 11
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1490+22C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.851+22C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1034+22C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1643+22C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1730+22C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1730+22C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1730+22C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*185+22C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1592+22C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1749+22C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1712+22C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1490+22C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1625+22C>G
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

11-68355514-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355514
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355514
    reference: chr 11
allele count: 24
allele frequency: 1.977424404712861e-4
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1749+22C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1712+22C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1730+22C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*185+22C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1592+22C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1490+22C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1490+22C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1643+22C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1730+22C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1034+22C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1625+22C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1730+22C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.851+22C>T
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8939
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3739
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: African
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

11-68355515-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355515
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355515
    reference: chr 11
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*185+23G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1490+23G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1643+23G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.851+23G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1592+23G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1730+23G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1625+23G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1490+23G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1730+23G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1730+23G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1712+23G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1034+23G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1749+23G>A
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8954
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3745
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

11-68355518-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355518
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355518
    reference: chr 11
allele count: 4
allele frequency: 3.295653033648617e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1730+26G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1592+26G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1730+26G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1490+26G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1643+26G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1730+26G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*185+26G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1749+26G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1490+26G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.851+26G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1034+26G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1625+26G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1712+26G>A
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP

11-68355518-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355518
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355518
    reference: chr 11
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*185+26G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1490+26G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1592+26G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1730+26G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1625+26G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1730+26G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1034+26G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1749+26G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1730+26G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1643+26G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.851+26G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1712+26G>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1490+26G>T
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8965
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46885
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/11-68355522-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355522
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355522
    reference: chr 11
allele count: 3
allele frequency: 2.472065658063878e-5
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1592+30C>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1749+30C>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1730+30C>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*185+30C>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1643+30C>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1490+30C>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1490+30C>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1730+30C>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1625+30C>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1034+30C>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1712+30C>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1730+30C>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.851+30C>A
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8940
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46764
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3770
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ

11-68355527-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355527
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355527
    reference: chr 11
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1730+35G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1730+35G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1034+35G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1730+35G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1749+35G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*185+35G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1490+35G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.851+35G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1625+35G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1712+35G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1643+35G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1490+35G>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1592+35G>C
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8943
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46480
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum

11-68355532-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355532
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355532
    reference: chr 11
allele count: 1
allele frequency: 8.241984669908513e-6
allele num: 121330
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1712+40C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1592+40C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.851+40C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1730+40C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1490+40C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1490+40C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*185+40C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1034+40C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1730+40C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1643+40C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1730+40C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1625+40C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1749+40C>T
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8974
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46283
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

11-68355544-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68355544
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68355544
    reference: chr 11
allele count: 1
allele frequency: 8.244838730954422e-6
allele num: 121288
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1730+52G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1643+52G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1625+52G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1749+52G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1034+52G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*185+52G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1730+52G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1490+52G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1730+52G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.851+52G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1592+52G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1490+52G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1712+52G>A
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3947
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9411
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45501
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: QD

11-68358080-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68358080
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68358080
    reference: chr 11
allele count: 1
allele frequency: 1.670676289762096e-5
allele num: 59856
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1713-48G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1491-48G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1626-48G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1593-48G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1731-48G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1644-48G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1731-48G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.852-48G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1491-48G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1035-48G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*186-48G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1731-48G>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1750-48G>A
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14664
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2887
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4085
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5537
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6870
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23256
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

11-68358081-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68358081
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68358081
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 59778
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1491-47C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1713-47C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1035-47C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1491-47C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1593-47C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1644-47C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1626-47C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1731-47C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1731-47C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.852-47C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*186-47C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1750-47C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1731-47C>T
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 23230
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6840
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1313
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14697
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5425
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum

11-68358082-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68358082
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68358082
    reference: chr 11
allele count: 0
allele frequency: 0.0e0
allele num: 60162
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1491-46T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1593-46T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1626-46T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1731-46T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*186-46T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1750-46T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1035-46T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1491-46T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1713-46T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1644-46T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1731-46T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.852-46T>A
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1731-46T>A
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6775
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23203
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14737
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP

11-68358082-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68358082
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68358082
    reference: chr 11
allele count: 6
allele frequency: 9.97307270370001e-5
allele num: 60162
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1491-46T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1731-46T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.852-46T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1713-46T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1593-46T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*186-46T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1750-46T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1491-46T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1731-46T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1731-46T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1626-46T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1035-46T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1644-46T>C
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14737
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6775
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23203
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 5295
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

11-68358100-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68358100
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68358100
    reference: chr 11
allele count: 1
allele frequency: 1.716679255647875e-5
allele num: 58252
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1644-28C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1626-28C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1035-28C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1731-28C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1731-28C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1731-28C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1491-28C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1593-28C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1491-28C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*186-28C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1713-28C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.852-28C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1750-28C>T
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15073
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21684
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4291
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6658
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

11-68358101-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68358101
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68358101
    reference: chr 11
allele count: 1
allele frequency: 1.728847550223021e-5
allele num: 57842
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1731-27C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1626-27C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1644-27C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1491-27C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1491-27C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1713-27C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1593-27C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1750-27C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*186-27C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1035-27C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1731-27C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1731-27C>T
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.852-27C>T
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1669
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4113
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 431
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6875
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21402
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14894
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3291
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: BaseQRankSum

11-68358103-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68358103
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68358103
    reference: chr 11
allele count: 2
allele frequency: 3.398932735121172e-5
allele num: 58842
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1713-25A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1644-25A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1750-25A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1626-25A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1491-25A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*186-25A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1593-25A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1491-25A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.852-25A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1731-25A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1035-25A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1731-25A>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1731-25A>G
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7374
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21251
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14674
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3834
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3321
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum

11-68358104-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68358104
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68358104
    reference: chr 11
allele count: 1
allele frequency: 1.693939085950469e-5
allele num: 59034
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1713-24C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1731-24C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1626-24C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1035-24C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1644-24C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1731-24C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1491-24C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1731-24C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1491-24C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1750-24C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1593-24C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*186-24C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.852-24C>G
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1693
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14467
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7667
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 839
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3655
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3329
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21061
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 482
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

11-68358106-CTTTTA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68358106
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68358101
    reference: chr 11
allele count: 22016
allele frequency: 2.835140495016354e-1
allele num: 77654
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1731-17_1731-13delATTTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1750-17_1750-13delATTTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1626-17_1626-13delATTTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1644-17_1644-13delATTTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1035-17_1035-13delATTTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*186-17_*186-13delATTTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1491-17_1491-13delATTTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1731-17_1731-13delATTTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1731-17_1731-13delATTTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1491-17_1491-13delATTTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1593-17_1593-13delATTTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1713-17_1713-13delATTTT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.852-17_852-13delATTTT
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18656
  bin: 7.5e0
  variant carriers: 2954
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 2.5e0
  variant carriers: 132
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 5.25e1
  variant carriers: 275
genotype depth: GenotypeDepth
  all individuals: 9957
  bin: 2.25e1
  variant carriers: 2660
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 9.75e1
  variant carriers: 189
genotype depth: GenotypeDepth
  all individuals: 6511
  bin: 1.75e1
  variant carriers: 5175
genotype depth: GenotypeDepth
  all individuals: 13755
  bin: 1.25e1
  variant carriers: 6634
genotype depth: GenotypeDepth
  all individuals: 1808
  bin: 3.25e1
  variant carriers: 934
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 7.75e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 5.75e1
  variant carriers: 214
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 4.75e1
  variant carriers: 431
genotype depth: GenotypeDepth
  all individuals: 754
  bin: 4.25e1
  variant carriers: 582
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 7.25e1
  variant carriers: 72
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 4051
  bin: 2.75e1
  variant carriers: 1454
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 6.25e1
  variant carriers: 126
genotype quality: GenotypeQuality
num of homozygotes: 2404
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
reference allele: CTTTTA
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: QD

11-68358116-G-GT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68358116
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68358117
    reference: chr 11
allele count: 369
allele frequency: 4.739153887647376e-3
allele num: 77862
alternate allele: GT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1731-5dupT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1731-5dupT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1626-5dupT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*186-5dupT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1593-5dupT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.852-5dupT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1035-5dupT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1644-5dupT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1491-5dupT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1491-5dupT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1750-5dupT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1731-5dupT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1713-5dupT
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 2.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 1.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 3.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 18937
  bin: 7.5e0
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 13495
  bin: 2.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 11522
  bin: 1.25e1
  variant carriers: 65
genotype quality: GenotypeQuality
num of homozygotes: 1
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

11-68358116-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68358116
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68358115
    reference: chr 11
allele count: 4
allele frequency: 5.137294187151627e-5
allele num: 77862
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1731-5delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1750-5delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1731-5delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1644-5delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1593-5delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.852-5delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1713-5delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1626-5delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1035-5delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1491-5delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*186-5delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1731-5delT
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1491-5delT
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11522
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18937
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13495
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Other
reference allele: GT
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum

11-68358123-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68358123
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68358123
    reference: chr 11
allele count: 1
allele frequency: 1.207904527226168e-5
allele num: 82788
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1731-5T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1593-5T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1750-5T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1713-5T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*186-5T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1731-5T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1626-5T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1035-5T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1731-5T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1491-5T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1491-5T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.852-5T>C
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1644-5T>C
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4045
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10322
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1027
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17147
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.1731-5T>C
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

11-68358141-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 68358141
    reference: chr 11
  end: Position
    type: ExactPosition
    position: 68358141
    reference: chr 11
allele count: 1
allele frequency: 1.118017977729082e-5
allele num: 89444
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000437329
  ensembl transcript: ENST00000529710
  gene symbol: PPP6R3
  hgvsc: ENST00000529710.1:c.1504C>G
  hgvsp: ENSP00000437329.1:p.Arg502Gly
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433565
  ensembl transcript: ENST00000527403
  gene symbol: PPP6R3
  hgvsc: ENST00000527403.2:c.1639C>G
  hgvsp: ENSP00000433565.1:p.Arg547Gly
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000110075
  ensembl transcript: ENST00000526307
  gene symbol: PPP6R3
  hgvsc: ENST00000526307.1:n.1763C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434429
  ensembl transcript: ENST00000534534
  gene symbol: PPP6R3
  hgvsc: ENST00000534534.1:c.1048C>G
  hgvsp: ENSP00000434429.1:p.Arg350Gly
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377388
  ensembl transcript: ENST00000393799
  gene symbol: PPP6R3
  hgvsc: ENST00000393799.2:c.1744C>G
  hgvsp: ENSP00000377388.2:p.Arg582Gly
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377390
  ensembl transcript: ENST00000393801
  gene symbol: PPP6R3
  hgvsc: ENST00000393801.3:c.1744C>G
  hgvsp: ENSP00000377390.3:p.Arg582Gly
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265637
  ensembl transcript: ENST00000265637
  gene symbol: PPP6R3
  hgvsc: ENST00000265637.4:c.1606C>G
  hgvsp: ENSP00000265637.4:p.Arg536Gly
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000265636
  ensembl transcript: ENST00000265636
  gene symbol: PPP6R3
  hgvsc: ENST00000265636.5:c.1504C>G
  hgvsp: ENSP00000265636.4:p.Arg502Gly
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000433058
  ensembl transcript: ENST00000524904
  gene symbol: PPP6R3
  hgvsc: ENST00000524904.1:c.1726C>G
  hgvsp: ENSP00000433058.1:p.Arg576Gly
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000377389
  ensembl transcript: ENST00000393800
  gene symbol: PPP6R3
  hgvsc: ENST00000393800.2:c.1744C>G
  hgvsp: ENSP00000377389.2:p.Arg582Gly
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000431415
  ensembl transcript: ENST00000524845
  gene symbol: PPP6R3
  hgvsc: ENST00000524845.1:c.1657C>G
  hgvsp: ENSP00000431415.1:p.Arg553Gly
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000434426
  ensembl transcript: ENST00000525421
  gene symbol: PPP6R3
  hgvsc: ENST00000525421.1:c.*199C>G
  variant of: http://identifiers.org/hgnc/1173
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000110075
  ensembl protein: ENSP00000436209
  ensembl transcript: ENST00000534190
  gene symbol: PPP6R3
  hgvsc: ENST00000534190.1:c.865C>G
  hgvsp: ENSP00000436209.1:p.Arg289Gly
  variant of: http://identifiers.org/hgnc/1173
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1981
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7250
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7111
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Arg582Gly
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

GenotypeDepth
all individuals: 7222
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1022
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 359
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 14031
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 198
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 2068
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 824
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21263
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4383
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15989
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 19
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3022
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6848
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3767
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2992
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 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: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16346
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 4.65e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.93e-1

QD
type: SiteQuality
SIO_000300: 1.338e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.22e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.88e0

DP
type: SiteQuality
SIO_000300: 2.164337e6

GenotypeDepth
all individuals: 10905
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 11675
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3124
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1436
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4369
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 162
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2967
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3766
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15988
bin: 9.75e1
variant carriers: 1

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

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

GenotypeQuality
all individuals: 6754
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3020
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 579
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20516
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16196
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66578
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-2

DP
type: SiteQuality
SIO_000300: 2.157559e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 1.022e1

FS
type: SiteQuality
SIO_000300: 6.6e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: 3.28e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

GenotypeDepth
all individuals: 7226
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1022
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2068
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 824
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15988
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2967
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3766
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4369
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 183
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 162
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20516
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3020
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6754
bin: 6.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8632
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16196
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501997656883655e-5
allele num: 66578
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: 902
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.21e0

MQRankSum
type: SiteQuality
SIO_000300: -7.9e-2

FS
type: SiteQuality
SIO_000300: 6.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.4e-2

QD
type: SiteQuality
SIO_000300: 1.022e1

VQSLOD
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SIO_000300: 3.28e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

DP
type: SiteQuality
SIO_000300: 2.157559e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16114
num of homozygotes: 0

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

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

Other
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allele frequency: 1.108647450110865e-3
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num of homozygotes: 0

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

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66506
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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QD
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ClippingRankSum
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MQ
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FS
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InbreedingCoeff
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SIO_000300: 3.0e-4

MQRankSum
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SIO_000300: 1.38e0

ReadPosRankSum
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SIO_000300: 7.65e-1

DP
type: SiteQuality
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VQSLOD
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SIO_000300: 3.09e-1

BaseQRankSum
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SIO_000300: -1.772e0

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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
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allele frequency: 1.247972045426183e-4
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European (Non-Finnish)
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allele frequency: 0.0e0
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MQRankSum
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SIO_000300: -1.42e0

BaseQRankSum
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QD
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ReadPosRankSum
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InbreedingCoeff
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SIO_000300: 4.7e-3

MQ
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SIO_000300: 6.0e1

FS
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ClippingRankSum
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SIO_000300: 2.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.159e-1

DP
type: SiteQuality
SIO_000300: 2.134646e6

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66416
num of homozygotes: 0

African
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allele frequency: 0.0e0
allele num: 10386
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 900
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

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

East Asian
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allele num: 8580
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.95e-1

VQSLOD
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SIO_000300: -2.024e-1

InbreedingCoeff
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SIO_000300: 4.6e-3

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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MQ
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SIO_000300: 5.966e1

BaseQRankSum
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SIO_000300: 6.13e0

MQRankSum
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SIO_000300: 1.84e0

QD
type: SiteQuality
SIO_000300: 1.04e1

DP
type: SiteQuality
SIO_000300: 2.132517e6

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 2
allele frequency: 1.926782273603083e-4
allele num: 10380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

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

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

South Asian
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num of homozygotes: 0

East Asian
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allele num: 8550
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

MQRankSum
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SIO_000300: -3.6e-2

BaseQRankSum
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ClippingRankSum
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FS
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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DP
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SIO_000300: 2.109643e6

GenotypeDepth
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2134
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.299908003679853e-4
allele num: 8696
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 7904
num of homozygotes: 0

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

Latino
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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FS
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ClippingRankSum
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QD
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GenotypeDepth
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variant carriers: 1

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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South Asian
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Latino
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Other
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European (Non-Finnish)
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InbreedingCoeff
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MQRankSum
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MQ
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VQSLOD
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FS
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DP
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QD
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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Latino
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allele frequency: 0.0e0
allele num: 400
num of homozygotes: 0

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

European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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Other
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VQSLOD
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ClippingRankSum
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DP
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MQ
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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InbreedingCoeff
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FS
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 3

GenotypeQuality
all individuals: 25
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GenotypeQuality
all individuals: 10
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 59

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 141
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GenotypeQuality
all individuals: 15
bin: 5.25e1
variant carriers: 2

European (Finnish)
type: Population
allele count: 5
allele frequency: 3.075030750307503e-3
allele num: 1626
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 1.239669421487603e-2
allele num: 242
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 4.642525533890436e-4
allele num: 2154
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 44
allele frequency: 4.996593231887349e-3
allele num: 8806
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 2.463054187192118e-3
allele num: 406
num of homozygotes: 0

South Asian
type: Population
allele count: 5
allele frequency: 6.322711178553364e-4
allele num: 7908
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.718e0

FS
type: SiteQuality
SIO_000300: 1.806e0

MQ
type: SiteQuality
SIO_000300: 5.972e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.6e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.93e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.179999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

DP
type: SiteQuality
SIO_000300: 4.44473e5

QD
type: SiteQuality
SIO_000300: 1.266e1

GenotypeDepth
all individuals: 132
bin: 8.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 670
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 14
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GenotypeQuality
all individuals: 262
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variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1638
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2206
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 412
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7910
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.095770326539557e-4
allele num: 9126
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 622
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 4.49087e5

BaseQRankSum
type: SiteQuality
SIO_000300: -5.79e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -9.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-3

FS
type: SiteQuality
SIO_000300: 1.74e0

VQSLOD
type: SiteQuality
SIO_000300: 2.11e0

QD
type: SiteQuality
SIO_000300: 1.191e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

GenotypeDepth
all individuals: 222
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variant carriers: 0

GenotypeDepth
all individuals: 161
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variant carriers: 0

GenotypeDepth
all individuals: 45
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 28
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GenotypeQuality
all individuals: 17
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7886
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.103265666372463e-4
allele num: 9064
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1636
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.18e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.79e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.62e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

FS
type: SiteQuality
SIO_000300: 4.4e-1

QD
type: SiteQuality
SIO_000300: 1.419e1

VQSLOD
type: SiteQuality
SIO_000300: 3.05e0

DP
type: SiteQuality
SIO_000300: 4.46728e5

BaseQRankSum
type: SiteQuality
SIO_000300: -5.74e-1

GenotypeDepth
all individuals: 243
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 203
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variant carriers: 0

GenotypeDepth
all individuals: 384
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variant carriers: 0

GenotypeQuality
all individuals: 343
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variant carriers: 0

GenotypeQuality
all individuals: 132
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GenotypeQuality
all individuals: 5285
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GenotypeQuality
all individuals: 699
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variant carriers: 0

GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 59
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GenotypeQuality
all individuals: 776
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GenotypeQuality
all individuals: 6
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 11
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1035
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GenotypeQuality
all individuals: 7
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 35
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.269680040629761e-4
allele num: 7876
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 414
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9058
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -2.433e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.58e-1

QD
type: SiteQuality
SIO_000300: 1.355e1

FS
type: SiteQuality
SIO_000300: 1.3767e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -2.561e0

DP
type: SiteQuality
SIO_000300: 4.46081e5

GenotypeDepth
all individuals: 154
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 76
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variant carriers: 0

GenotypeQuality
all individuals: 864
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GenotypeQuality
all individuals: 994
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GenotypeQuality
all individuals: 251
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variant carriers: 0

GenotypeQuality
all individuals: 46
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 131
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GenotypeQuality
all individuals: 13
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GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 51
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GenotypeQuality
all individuals: 3147
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 75
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GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 717
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 222
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GenotypeQuality
all individuals: 277
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GenotypeQuality
all individuals: 19
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GenotypeQuality
all individuals: 5089
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GenotypeQuality
all individuals: 324
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9000
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 242
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2192
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.274534794799898e-4
allele num: 7846
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.64e-1

DP
type: SiteQuality
SIO_000300: 4.42208e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.11e-1

VQSLOD
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SIO_000300: 3.42e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -3.116e0

QD
type: SiteQuality
SIO_000300: 9.98e0

MQRankSum
type: SiteQuality
SIO_000300: 4.54e-1

GenotypeDepth
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 880
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3141
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GenotypeQuality
all individuals: 216
bin: 9.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1628
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 2158
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 404
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 620
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 236
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -4.123e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.500000000000001e-3

MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.96427e5

BaseQRankSum
type: SiteQuality
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ClippingRankSum
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SIO_000300: 1.45e-1

QD
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SIO_000300: 1.662e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.85e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.202e0

FS
type: SiteQuality
SIO_000300: 2.066e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1400
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1254
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 7028
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
allele num: 512
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Other
type: Population
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allele frequency: 0.0e0
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European (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 count: 0
allele frequency: 0.0e0
allele num: 488
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South Asian
type: Population
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BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
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FS
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InbreedingCoeff
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MQRankSum
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VQSLOD
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MQ
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DP
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QD
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SIO_000300: 1.284e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.320655044902272e-4
allele num: 7572
num of homozygotes: 0

African
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num of homozygotes: 0

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

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

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 87
allele frequency: 2.13727705989289e-3
allele num: 40706
num of homozygotes: 0

East Asian
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South Asian
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allele frequency: 1.510574018126888e-3
allele num: 12578
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African
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allele num: 5918
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Other
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European (Finnish)
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allele count: 2
allele frequency: 4.050222762251924e-4
allele num: 4938
num of homozygotes: 0

Latino
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allele count: 8
allele frequency: 1.162790697674419e-3
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VQSLOD
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SIO_000300: 3.06e0

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

South Asian
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African
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Other
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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 frequency: 4.242321398269133e-5
allele num: 47144
num of homozygotes: 0

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

Latino
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allele frequency: 3.594536304816679e-4
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African
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European (Non-Finnish)
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Other
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East Asian
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European (Finnish)
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ClippingRankSum
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ReadPosRankSum
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MQ
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MQRankSum
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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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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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South Asian
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European (Finnish)
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Latino
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African
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East Asian
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European (Non-Finnish)
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MQRankSum
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FS
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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DP
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MQ
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InbreedingCoeff
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

East Asian
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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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South Asian
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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Other
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QD
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InbreedingCoeff
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VQSLOD
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FS
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ReadPosRankSum
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MQRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

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

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

Other
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num of homozygotes: 0

European (Non-Finnish)
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num of homozygotes: 0

Latino
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num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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East Asian
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Other
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DP
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ClippingRankSum
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BaseQRankSum
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MQ
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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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VQSLOD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

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

Other
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European (Non-Finnish)
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African
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South Asian
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Latino
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East Asian
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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QD
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FS
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MQ
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MQRankSum
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ClippingRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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European (Non-Finnish)
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South Asian
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East Asian
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African
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Latino
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ReadPosRankSum
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SIO_000300: 1.1e0

FS
type: SiteQuality
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VQSLOD
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MQ
type: SiteQuality
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ClippingRankSum
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QD
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BaseQRankSum
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MQRankSum
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SIO_000300: 4.94e-1

InbreedingCoeff
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DP
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
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allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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African
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Other
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DP
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SIO_000300: 1.404111e6

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

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

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

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

African
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VQSLOD
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SIO_000300: 8.65e-1

ReadPosRankSum
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MQRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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SIO_000300: 5.988e1

BaseQRankSum
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DP
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SIO_000300: 1.404782e6

QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 1

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

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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Latino
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num of homozygotes: 0

East Asian
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European (Non-Finnish)
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allele num: 66740
num of homozygotes: 0

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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num of homozygotes: 0

African
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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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South Asian
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DP
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ReadPosRankSum
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BaseQRankSum
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InbreedingCoeff
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FS
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MQ
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VQSLOD
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MQRankSum
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ClippingRankSum
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QD
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GenotypeDepth
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variant carriers: 0

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

East Asian
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allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
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SIO_000300: 5.24e0

DP
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QD
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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FS
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MQRankSum
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ClippingRankSum
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MQ
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GenotypeDepth
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variant carriers: 10

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 24

European (Non-Finnish)
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allele count: 21
allele frequency: 3.14776508678838e-4
allele num: 66714
num of homozygotes: 0

East Asian
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allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

South Asian
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African
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allele num: 10406
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QD
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
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MQ
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DP
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SIO_000300: 1.406835e6

BaseQRankSum
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SIO_000300: 5.24e0

MQRankSum
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SIO_000300: 1.22e-1

GenotypeDepth
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variant carriers: 0

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

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

East Asian
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allele frequency: 0.0e0
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Latino
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allele num: 11578
num of homozygotes: 0

European (Finnish)
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 906
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66718
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African
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InbreedingCoeff
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SIO_000300: 5.1e-3

FS
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ClippingRankSum
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DP
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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MQ
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BaseQRankSum
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SIO_000300: -2.367e0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 2

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156336725254394e-4
allele num: 8648
num of homozygotes: 0

Other
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African
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allele count: 3
allele frequency: 2.882952142994427e-4
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66712
num of homozygotes: 0

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 7.25e1
variant carriers: 0

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

European (Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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Other
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Latino
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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: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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DP
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MQ
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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MQRankSum
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QD
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BaseQRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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num of homozygotes: 0

African
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allele count: 0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
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allele num: 66708
num of homozygotes: 0

Other
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East Asian
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ClippingRankSum
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MQRankSum
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InbreedingCoeff
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FS
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VQSLOD
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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MQ
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
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num of homozygotes: 0

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

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

European (Non-Finnish)
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Other
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South Asian
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East Asian
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European (Finnish)
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Latino
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VQSLOD
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DP
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
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QD
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ClippingRankSum
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MQ
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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East Asian
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African
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European (Finnish)
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Latino
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South Asian
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European (Non-Finnish)
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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FS
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QD
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VQSLOD
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InbreedingCoeff
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MQ
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ReadPosRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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South Asian
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VQSLOD
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QD
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ClippingRankSum
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FS
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ReadPosRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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DP
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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South Asian
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Latino
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European (Non-Finnish)
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African
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East Asian
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InbreedingCoeff
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FS
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ClippingRankSum
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BaseQRankSum
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QD
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DP
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SIO_000300: 8.40005e5

VQSLOD
type: SiteQuality
SIO_000300: 7.72e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.58e0

GenotypeDepth
all individuals: 140
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variant carriers: 0

GenotypeDepth
all individuals: 24
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variant carriers: 0

GenotypeDepth
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 429
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GenotypeQuality
all individuals: 847
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variant carriers: 0

GenotypeQuality
all individuals: 1103
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GenotypeQuality
all individuals: 2575
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 772
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3065
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GenotypeQuality
all individuals: 1335
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variant carriers: 0

GenotypeQuality
all individuals: 185
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GenotypeQuality
all individuals: 3710
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7398
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GenotypeQuality
all individuals: 2886
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 505
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 7338
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1000
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 2

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5992
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4098
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4104
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.539572419651706e-5
allele num: 28252
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.68e-2

DP
type: SiteQuality
SIO_000300: 8.47834e5

MQRankSum
type: SiteQuality
SIO_000300: 3.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 9.448e0

QD
type: SiteQuality
SIO_000300: 1.135e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.03e0

GenotypeDepth
all individuals: 16
bin: 9.25e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 49
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 7175
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GenotypeQuality
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GenotypeQuality
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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: 1357
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 998
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variant carriers: 2

GenotypeQuality
all individuals: 391
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variant carriers: 0

GenotypeQuality
all individuals: 145
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GenotypeQuality
all individuals: 186
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variant carriers: 0

GenotypeQuality
all individuals: 2453
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7971
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 28798
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 4.739336492890995e-4
allele num: 4220
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4418
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10650
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.008e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.63e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.01e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.739e0

DP
type: SiteQuality
SIO_000300: 8.59175e5

QD
type: SiteQuality
SIO_000300: 1.081e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.17e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 9.65e-1

GenotypeDepth
all individuals: 49
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 137
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variant carriers: 0

GenotypeDepth
all individuals: 4175
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variant carriers: 0

GenotypeQuality
all individuals: 6707
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GenotypeQuality
all individuals: 187
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 419
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GenotypeQuality
all individuals: 997
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variant carriers: 1

GenotypeQuality
all individuals: 2356
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variant carriers: 0

GenotypeQuality
all individuals: 20462
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 782
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variant carriers: 0

GenotypeQuality
all individuals: 1373
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variant carriers: 0

GenotypeQuality
all individuals: 689
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GenotypeQuality
all individuals: 143
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variant carriers: 0

GenotypeQuality
all individuals: 1201
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GenotypeQuality
all individuals: 3618
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 338
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variant carriers: 0

GenotypeQuality
all individuals: 4352
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 516
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GenotypeQuality
all individuals: 2814
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8228
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4156
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4452
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 3.457097421005324e-5
allele num: 28926
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4222
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6084
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10666
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.197e0

DP
type: SiteQuality
SIO_000300: 8.67221e5

QD
type: SiteQuality
SIO_000300: 8.44e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.55e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.97e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e0

GenotypeDepth
all individuals: 977
bin: 3.75e1
variant carriers: 682

GenotypeDepth
all individuals: 36
bin: 9.25e1
variant carriers: 32

GenotypeDepth
all individuals: 141
bin: 6.75e1
variant carriers: 101

GenotypeQuality
all individuals: 381
bin: 5.75e1
variant carriers: 227

GenotypeQuality
all individuals: 220
bin: 8.75e1
variant carriers: 118

GenotypeQuality
all individuals: 729
bin: 1.75e1
variant carriers: 173

GenotypeQuality
all individuals: 1680
bin: 3.75e1
variant carriers: 315

GenotypeQuality
all individuals: 1648
bin: 2.5e0
variant carriers: 21

GenotypeQuality
all individuals: 585
bin: 4.75e1
variant carriers: 241

GenotypeQuality
all individuals: 722
bin: 1.25e1
variant carriers: 91

GenotypeQuality
all individuals: 1737
bin: 7.5e0
variant carriers: 33

GenotypeQuality
all individuals: 3118
bin: 3.25e1
variant carriers: 331

GenotypeQuality
all individuals: 14709
bin: 2.25e1
variant carriers: 171

GenotypeQuality
all individuals: 453
bin: 7.75e1
variant carriers: 77

GenotypeQuality
all individuals: 250
bin: 9.25e1
variant carriers: 121

GenotypeQuality
all individuals: 351
bin: 8.25e1
variant carriers: 98

GenotypeQuality
all individuals: 1265
bin: 6.75e1
variant carriers: 119

GenotypeQuality
all individuals: 501
bin: 5.25e1
variant carriers: 264

GenotypeQuality
all individuals: 466
bin: 7.25e1
variant carriers: 81

GenotypeQuality
all individuals: 2745
bin: 2.75e1
variant carriers: 339

GenotypeQuality
all individuals: 796
bin: 4.25e1
variant carriers: 387

GenotypeQuality
all individuals: 8056
bin: 6.25e1
variant carriers: 139

GenotypeQuality
all individuals: 20076
bin: 9.75e1
variant carriers: 19442

East Asian
type: Population
allele count: 1645
allele frequency: 2.914599574769667e-1
allele num: 5644
num of homozygotes: 183

South Asian
type: Population
allele count: 2391
allele frequency: 1.967577353522054e-1
allele num: 12152
num of homozygotes: 223

European (Non-Finnish)
type: Population
allele count: 12843
allele frequency: 3.181007579135087e-1
allele num: 40374
num of homozygotes: 1506

Other
type: Population
allele count: 163
allele frequency: 2.570977917981073e-1
allele num: 634
num of homozygotes: 17

African
type: Population
allele count: 1800
allele frequency: 2.446982055464927e-1
allele num: 7356
num of homozygotes: 166

Latino
type: Population
allele count: 2223
allele frequency: 3.340847610459874e-1
allele num: 6654
num of homozygotes: 247

European (Finnish)
type: Population
allele count: 951
allele frequency: 1.964876033057851e-1
allele num: 4840
num of homozygotes: 62

MQRankSum
type: SiteQuality
SIO_000300: -2.306e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.72e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -1.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e-1

FS
type: SiteQuality
SIO_000300: 2.661e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.95e-1

MQ
type: SiteQuality
SIO_000300: 5.057e1

VQSLOD
type: SiteQuality
SIO_000300: 3.07e0

DP
type: SiteQuality
SIO_000300: 9.9921e5

QD
type: SiteQuality
SIO_000300: 1.249e1

GenotypeDepth
all individuals: 94
bin: 6.75e1
variant carriers: 6

GenotypeDepth
all individuals: 668
bin: 3.75e1
variant carriers: 26

GenotypeDepth
all individuals: 55
bin: 7.75e1
variant carriers: 3

GenotypeQuality
all individuals: 19546
bin: 2.25e1
variant carriers: 3

GenotypeQuality
all individuals: 4013
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2987
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1457
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 862
bin: 1.25e1
variant carriers: 2

GenotypeQuality
all individuals: 722
bin: 2.5e0
variant carriers: 4

GenotypeQuality
all individuals: 1769
bin: 9.75e1
variant carriers: 341

GenotypeQuality
all individuals: 450
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 1205
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1995
bin: 4.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14931
bin: 6.25e1
variant carriers: 8

GenotypeQuality
all individuals: 260
bin: 9.25e1
variant carriers: 9

GenotypeQuality
all individuals: 1442
bin: 4.25e1
variant carriers: 4

GenotypeQuality
all individuals: 3332
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2104
bin: 6.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1512
bin: 7.5e0
variant carriers: 1

GenotypeQuality
all individuals: 677
bin: 7.25e1
variant carriers: 5

GenotypeQuality
all individuals: 498
bin: 5.75e1
variant carriers: 6

GenotypeQuality
all individuals: 198
bin: 8.75e1
variant carriers: 6

GenotypeQuality
all individuals: 697
bin: 7.75e1
variant carriers: 2

South Asian
type: Population
allele count: 112
allele frequency: 9.221142763049564e-3
allele num: 12146
num of homozygotes: 0

Latino
type: Population
allele count: 11
allele frequency: 1.58273381294964e-3
allele num: 6950
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 239
allele frequency: 5.977689960482217e-3
allele num: 39982
num of homozygotes: 1

Other
type: Population
allele count: 5
allele frequency: 7.692307692307693e-3
allele num: 650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5778
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.68889486421081e-4
allele num: 7438
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4918
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.152e1

MQRankSum
type: SiteQuality
SIO_000300: 8.73e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.93085e5

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.88e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 4.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

GenotypeDepth
all individuals: 20
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27
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variant carriers: 0

GenotypeDepth
all individuals: 87
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variant carriers: 0

GenotypeQuality
all individuals: 1769
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 722
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GenotypeQuality
all individuals: 1512
bin: 7.5e0
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GenotypeQuality
all individuals: 19546
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1995
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2987
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1457
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3332
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 677
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1442
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2104
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 862
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1205
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 198
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variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14931
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4013
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 260
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GenotypeQuality
all individuals: 697
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7438
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.877697841726619e-4
allele num: 6950
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.00225101295583e-5
allele num: 39982
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5778
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4918
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12146
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.73e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.152e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.88e-2

DP
type: SiteQuality
SIO_000300: 9.93085e5

VQSLOD
type: SiteQuality
SIO_000300: 4.97e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.0e-3

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

GenotypeDepth
all individuals: 6058
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1898
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variant carriers: 0

GenotypeDepth
all individuals: 83
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variant carriers: 0

GenotypeDepth
all individuals: 20
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variant carriers: 0

GenotypeDepth
all individuals: 26
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variant carriers: 0

GenotypeDepth
all individuals: 250
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variant carriers: 0

GenotypeQuality
all individuals: 2698
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3559
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19686
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 957
bin: 7.5e0
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GenotypeQuality
all individuals: 2436
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 765
bin: 7.25e1
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GenotypeQuality
all individuals: 267
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GenotypeQuality
all individuals: 19876
bin: 6.25e1
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GenotypeQuality
all individuals: 2992
bin: 2.75e1
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GenotypeQuality
all individuals: 556
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GenotypeQuality
all individuals: 1138
bin: 4.25e1
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GenotypeQuality
all individuals: 58
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GenotypeQuality
all individuals: 477
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GenotypeQuality
all individuals: 1452
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GenotypeQuality
all individuals: 205
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GenotypeQuality
all individuals: 781
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GenotypeQuality
all individuals: 166
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GenotypeQuality
all individuals: 411
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1438
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 684
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.282380097460887e-4
allele num: 7798
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5136
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6220
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42874
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.953e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -5.373e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.06e-1

DP
type: SiteQuality
SIO_000300: 1.029037e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-1

GenotypeDepth
all individuals: 24673
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 102
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 20
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 52
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 88
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 218
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2023
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2566
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1447
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 308
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27405
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2141
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 466
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17460
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1308
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13106
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46302
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.456876456876457e-4
allele num: 6864
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8454
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 732
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

QD
type: SiteQuality
SIO_000300: 2.98e0

VQSLOD
type: SiteQuality
SIO_000300: -1.032e0

FS
type: SiteQuality
SIO_000300: 1.309e0

DP
type: SiteQuality
SIO_000300: 1.128201e6

BaseQRankSum
type: SiteQuality
SIO_000300: -8.62e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.2e-1

MQ
type: SiteQuality
SIO_000300: 5.477e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.96e-1