3-167405371-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405371
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405371
    reference: chr 3
allele count: 1
allele frequency: 8.416799932665601e-6
allele num: 118810
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.474+32C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.285+32C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.474+32C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-267C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.474+32C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.474+32C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.474+32C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.474+32C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.474+32C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.474+32C>T
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4256
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25069
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1111
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2144
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3383
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4850
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1480
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1206
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 969
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQ

3-167405391-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405391
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405391
    reference: chr 3
allele count: 7
allele frequency: 5.840731593351578e-5
allele num: 119848
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.474+12A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.474+12A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.474+12A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-287A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.474+12A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.474+12A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.474+12A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.285+12A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.474+12A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.474+12A>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1015
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4387
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1114
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17687
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1667
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 860
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6509
  bin: 9.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

3-167405394-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405394
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405394
    reference: chr 3
allele count: 19
allele frequency: 1.58378207158695e-4
allele num: 119966
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.285+9A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.474+9A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-290A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.474+9A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.474+9A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.474+9A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.474+9A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.474+9A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.474+9A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.474+9A>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4388
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28103
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 842
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1115
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17797
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6518
  bin: 9.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 366
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum

3-167405407-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405407
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405407
    reference: chr 3
allele count: 1
allele frequency: 8.313795912937929e-6
allele num: 120282
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.470G>A
  hgvsp: ENSP00000420266.2:p.Arg157His
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.470G>A
  hgvsp: ENSP00000376506.2:p.Arg157His
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.470G>A
  hgvsp: ENSP00000418317.2:p.Arg157His
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.470G>A
  hgvsp: ENSP00000420553.2:p.Arg157His
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.470G>A
  hgvsp: ENSP00000420021.1:p.Arg157His
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.470G>A
  hgvsp: ENSP00000417202.1:p.Arg157His
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-303G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.470G>A
  hgvsp: ENSP00000417876.1:p.Arg157His
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.281G>A
  hgvsp: ENSP00000417309.1:p.Arg94His
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.470G>A
  hgvsp: ENSP00000417118.2:p.Arg157His
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1112
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1674
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28189
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4450
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18317
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6503
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Arg157His
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD

3-167405418-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405418
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405418
    reference: chr 3
allele count: 3
allele frequency: 2.492439599880363e-5
allele num: 120364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.459A>G
  hgvsp: ENST00000487947.2:c.459A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.459A>G
  hgvsp: ENST00000470131.1:c.459A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.459A>G
  hgvsp: ENST00000461494.1:c.459A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.459A>G
  hgvsp: ENST00000475915.2:c.459A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.270A>G
  hgvsp: ENST00000492396.1:c.270A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.459A>G
  hgvsp: ENST00000471885.1:c.459A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.459A>G
  hgvsp: ENST00000497056.2:c.459A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.459A>G
  hgvsp: ENST00000473645.2:c.459A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-314A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.459A>G
  hgvsp: ENST00000392750.2:c.459A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4429
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28107
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18596
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6498
  bin: 9.75e1
  variant carriers: 3
hgvs: p.Gln153Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: T
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

3-167405436-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405436
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405436
    reference: chr 3
allele count: 2
allele frequency: 1.663921196692125e-5
allele num: 120198
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.441T>C
  hgvsp: ENST00000497056.2:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.441T>C
  hgvsp: ENST00000461494.1:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-332T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.441T>C
  hgvsp: ENST00000475915.2:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.441T>C
  hgvsp: ENST00000471885.1:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.252T>C
  hgvsp: ENST00000492396.1:c.252T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.441T>C
  hgvsp: ENST00000473645.2:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.441T>C
  hgvsp: ENST00000487947.2:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.441T>C
  hgvsp: ENST00000470131.1:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.441T>C
  hgvsp: ENST00000392750.2:c.441T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4413
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asn147Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

3-167405438-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405438
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405438
    reference: chr 3
allele count: 1
allele frequency: 8.326671995736744e-6
allele num: 120096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.439A>G
  hgvsp: ENSP00000417876.1:p.Asn147Asp
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: incomplete_terminal_codon_variant
  consequence: coding_sequence_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.439A>G
  hgvsp: ENST00000462725.2:c.439A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.250A>G
  hgvsp: ENSP00000417309.1:p.Asn84Asp
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.439A>G
  hgvsp: ENSP00000417118.2:p.Asn147Asp
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.439A>G
  hgvsp: ENSP00000420266.2:p.Asn147Asp
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.439A>G
  hgvsp: ENSP00000420021.1:p.Asn147Asp
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.439A>G
  hgvsp: ENSP00000420553.2:p.Asn147Asp
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.439A>G
  hgvsp: ENSP00000417202.1:p.Asn147Asp
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.439A>G
  hgvsp: ENSP00000376506.2:p.Asn147Asp
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.439A>G
  hgvsp: ENSP00000418317.2:p.Asn147Asp
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-334A>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4414
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18721
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1660
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27805
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn147Asp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: DP

3-167405443-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405443
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405443
    reference: chr 3
allele count: 1
allele frequency: 8.33152816889674e-6
allele num: 120026
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.434T>C
  hgvsp: ENSP00000420021.1:p.Val145Ala
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.434T>C
  hgvsp: ENSP00000417118.2:p.Val145Ala
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.434T>C
  hgvsp: ENSP00000417876.1:p.Val145Ala
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.245T>C
  hgvsp: ENSP00000417309.1:p.Val82Ala
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-339T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.434T>C
  hgvsp: ENSP00000420266.2:p.Val145Ala
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.434T>C
  hgvsp: ENSP00000420424.2:p.Val145Ala
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.434T>C
  hgvsp: ENSP00000376506.2:p.Val145Ala
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.434T>C
  hgvsp: ENSP00000418317.2:p.Val145Ala
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.434T>C
  hgvsp: ENSP00000417202.1:p.Val145Ala
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.434T>C
  hgvsp: ENSP00000420553.2:p.Val145Ala
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1446
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4415
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 651
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18718
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1454
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val145Ala
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ

3-167405461-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405461
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405461
    reference: chr 3
allele count: 1
allele frequency: 8.412693071305987e-6
allele num: 118868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.416A>G
  hgvsp: ENSP00000420424.2:p.Lys139Arg
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.416A>G
  hgvsp: ENSP00000420553.2:p.Lys139Arg
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.227A>G
  hgvsp: ENSP00000417309.1:p.Lys76Arg
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.416A>G
  hgvsp: ENSP00000376506.2:p.Lys139Arg
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.416A>G
  hgvsp: ENSP00000417876.1:p.Lys139Arg
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.416A>G
  hgvsp: ENSP00000417202.1:p.Lys139Arg
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.416A>G
  hgvsp: ENSP00000418317.2:p.Lys139Arg
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.416A>G
  hgvsp: ENSP00000417118.2:p.Lys139Arg
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.416A>G
  hgvsp: ENSP00000420266.2:p.Lys139Arg
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-357A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.416A>G
  hgvsp: ENSP00000420021.1:p.Lys139Arg
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18566
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26355
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 452
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1308
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1445
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1654
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys139Arg
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

3-167405481-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405481
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405481
    reference: chr 3
allele count: 4
allele frequency: 3.474876641879213e-5
allele num: 115112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.396G>A
  hgvsp: ENST00000492139.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.207G>A
  hgvsp: ENST00000492396.1:c.207G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-377G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.396G>A
  hgvsp: ENST00000470131.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.396G>A
  hgvsp: ENST00000461494.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.396G>A
  hgvsp: ENST00000462725.2:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.396G>A
  hgvsp: ENST00000497056.2:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.396G>A
  hgvsp: ENST00000475915.2:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.396G>A
  hgvsp: ENST00000471885.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.396G>A
  hgvsp: ENST00000473645.2:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.396G>A
  hgvsp: ENST00000487947.2:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.396G>A
  hgvsp: ENST00000392750.2:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21397
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2987
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 555
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4780
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.396G>A
num of homozygotes: 0
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff

3-167405486-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405486
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405486
    reference: chr 3
allele count: 2
allele frequency: 1.757006061670913e-5
allele num: 113830
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.396-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.396-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.396-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.396-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.396-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.396-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-382A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.396-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.207-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.396-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.396-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.396-5A>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1424
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3609
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6453
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 829
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19557
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.396-5A>G
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: T
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

3-167405503-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405503
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405503
    reference: chr 3
allele count: 1
allele frequency: 9.151140232072917e-6
allele num: 109276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.396-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.396-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.396-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.396-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.396-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.396-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.396-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.207-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.396-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.396-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.396-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-399T>C
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1566
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 554
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12200
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5444
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11286
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1108
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 828
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

3-167405504-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405504
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405504
    reference: chr 3
allele count: 1
allele frequency: 9.163719003720471e-6
allele num: 109126
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.396-23A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.396-23A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.396-23A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.396-23A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.396-23A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.396-23A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.396-23A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.396-23A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-400A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.396-23A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.396-23A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.207-23A>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5511
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11789
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10795
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15837
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

3-167405504-TATCAGCTACATTTGAAAGAAATTTGTGAGAGAAAAGAAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405504
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405465
    reference: chr 3
allele count: 112
allele frequency: 1.026336528416693e-3
allele num: 109126
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 1106
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 550
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 3.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 480
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4754
  bin: 1.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 3267
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 4.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 11789
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 10795
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5511
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15837
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 6.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 540
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 2
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: TATCAGCTACATTTGAAAGAAATTTGTGAGAGAAAAGAAC
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

3-167405511-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405511
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405511
    reference: chr 3
allele count: 2
allele frequency: 1.869228756215186e-5
allele num: 106996
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.396-30A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.396-30A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.396-30A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-407A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.396-30A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.396-30A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.207-30A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.396-30A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.396-30A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.396-30A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.396-30A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.396-30A>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1098
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8633
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6030
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 781
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8000
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7650
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

3-167405515-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405515
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405515
    reference: chr 3
allele count: 1
allele frequency: 9.438414346389807e-6
allele num: 105950
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.396-34A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.396-34A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.396-34A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.207-34A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.396-34A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-411A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.396-34A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.396-34A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.396-34A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.396-34A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.396-34A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.396-34A>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7157
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6361
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 923
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2432
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19005
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
reference allele: T
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum

3-167405516-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405516
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405516
    reference: chr 3
allele count: 1
allele frequency: 9.52072662185578e-6
allele num: 105034
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.396-35A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.396-35A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-412A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.396-35A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.207-35A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.396-35A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.396-35A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.396-35A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.396-35A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.396-35A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.396-35A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.396-35A>T
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11768
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5641
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18833
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6165
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6708
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1011
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: DP

3-167405524-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405524
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405524
    reference: chr 3
allele count: 1
allele frequency: 9.764671418806758e-6
allele num: 102410
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.207-43T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.396-43T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.396-43T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.396-43T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.396-43T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-420T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.396-43T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.396-43T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.396-43T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.396-43T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.396-43T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.396-43T>C
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 17943
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5725
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1087
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13749
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1997
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7949
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3976
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1410
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1096
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD

3-167405529-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405529
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405529
    reference: chr 3
allele count: 40
allele frequency: 3.980654021455725e-4
allele num: 100486
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.396-48C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.396-48C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.396-48C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.396-48C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.396-48C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.396-48C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.207-48C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.396-48C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.396-48C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-425C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.396-48C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.396-48C>T
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6545
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8590
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17424
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13614
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

3-167405529-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167405529
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167405529
    reference: chr 3
allele count: 2
allele frequency: 1.990327010727862e-5
allele num: 100486
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.396-48C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.396-48C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.396-48C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.396-48C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.396-48C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.396-48C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.396-48C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.396-48C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.396-48C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.337-425C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.396-48C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.207-48C>A
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8590
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6545
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13614
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1409
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1093
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17424
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD

3-167413333-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413333
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413334
    reference: chr 3
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.395+50dupG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.395+50dupG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.206+50dupG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.395+50dupG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.395+50dupG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.395+50dupG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.395+50dupG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.395+50dupG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.336+50dupG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.395+50dupG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.395+50dupG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.395+50dupG
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8335
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10377
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2975
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

3-167413337-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413337
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413337
    reference: chr 3
allele count: 2
allele frequency: 1.648233917357551e-5
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.395+47G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.395+47G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.206+47G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.395+47G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.336+47G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.395+47G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.395+47G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.395+47G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.395+47G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.395+47G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.395+47G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.395+47G>A
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8980
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2977
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10379
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 703
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1571
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2932
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5759
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

3-167413338-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413338
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413338
    reference: chr 3
allele count: 356
allele frequency: 2.933614608741512e-3
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.395+46C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.336+46C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.395+46C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.395+46C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.395+46C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.395+46C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.395+46C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.395+46C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.395+46C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.395+46C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.206+46C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.395+46C>T
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8974
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 10378
  bin: 3.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 5761
  bin: 4.75e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 6.25e1
  variant carriers: 28
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 7.25e1
  variant carriers: 35
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 7.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 8363
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 710
  bin: 8.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2942
  bin: 9.75e1
  variant carriers: 79
genotype depth: GenotypeDepth
  all individuals: 2969
  bin: 5.75e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 7474
  bin: 4.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 8.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 4196
  bin: 5.25e1
  variant carriers: 26
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Non-Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

3-167413352-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413352
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413352
    reference: chr 3
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.336+32C>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.395+32C>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.395+32C>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.395+32C>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.206+32C>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.395+32C>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.395+32C>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.395+32C>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.395+32C>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.395+32C>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.395+32C>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.395+32C>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1918
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1191
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5766
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8454
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

3-167413353-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413353
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413353
    reference: chr 3
allele count: 4
allele frequency: 3.295707341188102e-5
allele num: 121370
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.395+31T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.395+31T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.395+31T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.395+31T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.395+31T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.395+31T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.395+31T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.395+31T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.206+31T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.395+31T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.336+31T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.395+31T>C
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10446
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff

3-167413354-AAAG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413354
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413351
    reference: chr 3
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.395+27_395+29delCTT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.395+27_395+29delCTT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.395+27_395+29delCTT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.395+27_395+29delCTT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.395+27_395+29delCTT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.206+27_206+29delCTT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.336+27_336+29delCTT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.395+27_395+29delCTT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.395+27_395+29delCTT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.395+27_395+29delCTT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.395+27_395+29delCTT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.395+27_395+29delCTT
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8469
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5767
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9018
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: AAAG
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQRankSum

3-167413360-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413360
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413360
    reference: chr 3
allele count: 3
allele frequency: 2.47161759132627e-5
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.395+24C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.395+24C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.336+24C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.395+24C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.206+24C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.395+24C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.395+24C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.395+24C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.395+24C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.395+24C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.395+24C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.395+24C>A
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5768
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

3-167413373-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413373
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413373
    reference: chr 3
allele count: 1
allele frequency: 8.237910865804433e-6
allele num: 121390
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.395+11A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.395+11A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.206+11A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.395+11A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.395+11A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.336+11A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.395+11A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.395+11A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.395+11A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.395+11A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.395+11A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.395+11A>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10463
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2961
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/3-167413402-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413402
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413402
    reference: chr 3
allele count: 2
allele frequency: 1.647473599235572e-5
allele num: 121398
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.377G>T
  hgvsp: ENSP00000418317.2:p.Arg126Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*325G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.377G>T
  hgvsp: ENSP00000417202.1:p.Arg126Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.377G>T
  hgvsp: ENSP00000417876.1:p.Arg126Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.318G>T
  hgvsp: ENSP00000420308.1:p.Arg107Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.377G>T
  hgvsp: ENSP00000420014.1:p.Arg126Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.377G>T
  hgvsp: ENSP00000420266.2:p.Arg126Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.377G>T
  hgvsp: ENSP00000420021.1:p.Arg126Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.377G>T
  hgvsp: ENSP00000417118.2:p.Arg126Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.377G>T
  hgvsp: ENSP00000420424.2:p.Arg126Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.377G>T
  hgvsp: ENSP00000376506.2:p.Arg126Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.188G>T
  hgvsp: ENSP00000417309.1:p.Arg63Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.377G>T
  hgvsp: ENSP00000420553.2:p.Arg126Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.1101G>T
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5770
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg126Met
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum

3-167413408-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413408
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413408
    reference: chr 3
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.371G>A
  hgvsp: ENSP00000420014.1:p.Arg124Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.371G>A
  hgvsp: ENSP00000417876.1:p.Arg124Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.1095G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*319G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.182G>A
  hgvsp: ENSP00000417309.1:p.Arg61Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.371G>A
  hgvsp: ENSP00000417202.1:p.Arg124Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.371G>A
  hgvsp: ENSP00000420424.2:p.Arg124Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.371G>A
  hgvsp: ENSP00000376506.2:p.Arg124Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.371G>A
  hgvsp: ENSP00000420553.2:p.Arg124Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.371G>A
  hgvsp: ENSP00000417118.2:p.Arg124Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.371G>A
  hgvsp: ENSP00000420266.2:p.Arg124Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.371G>A
  hgvsp: ENSP00000418317.2:p.Arg124Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.312G>A
  hgvsp: ENSP00000420308.1:p.Arg105Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.371G>A
  hgvsp: ENSP00000420021.1:p.Arg124Lys
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10464
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg124Lys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQ

3-167413416-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413416
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413416
    reference: chr 3
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.363C>G
  hgvsp: ENSP00000417118.2:p.Ile121Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.363C>G
  hgvsp: ENSP00000417876.1:p.Ile121Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.363C>G
  hgvsp: ENSP00000418317.2:p.Ile121Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.304C>G
  hgvsp: ENSP00000420308.1:p.Ile102Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.363C>G
  hgvsp: ENSP00000420014.1:p.Ile121Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.363C>G
  hgvsp: ENSP00000420266.2:p.Ile121Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.363C>G
  hgvsp: ENSP00000417202.1:p.Ile121Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.174C>G
  hgvsp: ENSP00000417309.1:p.Ile58Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.363C>G
  hgvsp: ENSP00000420424.2:p.Ile121Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.363C>G
  hgvsp: ENSP00000420553.2:p.Ile121Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.363C>G
  hgvsp: ENSP00000376506.2:p.Ile121Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*311C>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.363C>G
  hgvsp: ENSP00000420021.1:p.Ile121Met
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.1087C>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7484
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9015
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile121Met
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum

3-167413436-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413436
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413436
    reference: chr 3
allele count: 1
allele frequency: 8.237367996177861e-6
allele num: 121398
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.343A>G
  hgvsp: ENSP00000420553.2:p.Ser115Gly
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.343A>G
  hgvsp: ENSP00000420021.1:p.Ser115Gly
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.154A>G
  hgvsp: ENSP00000417309.1:p.Ser52Gly
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.343A>G
  hgvsp: ENSP00000418317.2:p.Ser115Gly
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.343A>G
  hgvsp: ENSP00000417202.1:p.Ser115Gly
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.343A>G
  hgvsp: ENSP00000420014.1:p.Ser115Gly
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.343A>G
  hgvsp: ENSP00000376506.2:p.Ser115Gly
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.1067A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.343A>G
  hgvsp: ENSP00000420424.2:p.Ser115Gly
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.343A>G
  hgvsp: ENSP00000417876.1:p.Ser115Gly
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*291A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.343A>G
  hgvsp: ENSP00000420266.2:p.Ser115Gly
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.343A>G
  hgvsp: ENSP00000417118.2:p.Ser115Gly
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.284A>G
  hgvsp: ENSP00000420308.1:p.Ser96Gly
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5771
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser115Gly
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

3-167413456-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413456
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413456
    reference: chr 3
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*271G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.323G>A
  hgvsp: ENSP00000418317.2:p.Arg108Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.323G>A
  hgvsp: ENSP00000420553.2:p.Arg108Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.323G>A
  hgvsp: ENSP00000417202.1:p.Arg108Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.134G>A
  hgvsp: ENSP00000417309.1:p.Arg45Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.323G>A
  hgvsp: ENSP00000376506.2:p.Arg108Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.323G>A
  hgvsp: ENSP00000417876.1:p.Arg108Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.1047G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.264G>A
  hgvsp: ENSP00000420308.1:p.Arg89Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.323G>A
  hgvsp: ENSP00000420424.2:p.Arg108Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.323G>A
  hgvsp: ENSP00000420021.1:p.Arg108Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.323G>A
  hgvsp: ENSP00000417118.2:p.Arg108Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.323G>A
  hgvsp: ENSP00000420014.1:p.Arg108Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.323G>A
  hgvsp: ENSP00000420266.2:p.Arg108Gln
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8503
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2897
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg108Gln
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ

3-167413466-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413466
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413466
    reference: chr 3
allele count: 3
allele frequency: 2.471251112063001e-5
allele num: 121396
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.313G>A
  hgvsp: ENSP00000420021.1:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.313G>A
  hgvsp: ENSP00000417202.1:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.313G>A
  hgvsp: ENSP00000420014.1:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.124G>A
  hgvsp: ENSP00000417309.1:p.Glu42Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.313G>A
  hgvsp: ENSP00000376506.2:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.313G>A
  hgvsp: ENSP00000420424.2:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.254G>A
  hgvsp: ENSP00000420308.1:p.Glu86Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.313G>A
  hgvsp: ENSP00000418317.2:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.1037G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.313G>A
  hgvsp: ENSP00000417118.2:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*261G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.313G>A
  hgvsp: ENSP00000420553.2:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.313G>A
  hgvsp: ENSP00000417876.1:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.313G>A
  hgvsp: ENSP00000420266.2:p.Glu105Lys
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2896
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7483
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu105Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

3-167413467-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413467
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413467
    reference: chr 3
allele count: 2
allele frequency: 1.647500741375333e-5
allele num: 121396
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.312C>T
  hgvsp: ENST00000487947.2:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.312C>T
  hgvsp: ENST00000475915.2:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.1036C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.312C>T
  hgvsp: ENST00000462725.2:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.312C>T
  hgvsp: ENST00000392750.2:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.312C>T
  hgvsp: ENST00000497056.2:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.312C>T
  hgvsp: ENST00000473645.2:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.312C>T
  hgvsp: ENST00000470131.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.253C>T
  hgvsp: ENST00000479121.1:c.253C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.123C>T
  hgvsp: ENST00000492396.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.312C>T
  hgvsp: ENST00000492139.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.312C>T
  hgvsp: ENST00000461494.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*260C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.312C>T
  hgvsp: ENST00000471885.1:c.312C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2163
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5771
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2958
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn104Asn
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum

3-167413468-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413468
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413468
    reference: chr 3
allele count: 5
allele frequency: 4.118751853438334e-5
allele num: 121396
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.252A>G
  hgvsp: ENSP00000420308.1:p.Asn85Ser
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.311A>G
  hgvsp: ENSP00000420266.2:p.Asn104Ser
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.311A>G
  hgvsp: ENSP00000418317.2:p.Asn104Ser
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.311A>G
  hgvsp: ENSP00000417876.1:p.Asn104Ser
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.311A>G
  hgvsp: ENSP00000420553.2:p.Asn104Ser
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.1035A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.311A>G
  hgvsp: ENSP00000376506.2:p.Asn104Ser
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*259A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.311A>G
  hgvsp: ENSP00000420424.2:p.Asn104Ser
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.311A>G
  hgvsp: ENSP00000420021.1:p.Asn104Ser
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.311A>G
  hgvsp: ENSP00000417202.1:p.Asn104Ser
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.122A>G
  hgvsp: ENSP00000417309.1:p.Asn41Ser
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.311A>G
  hgvsp: ENSP00000417118.2:p.Asn104Ser
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.311A>G
  hgvsp: ENSP00000420014.1:p.Asn104Ser
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5772
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn104Ser
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
population: Latino
reference allele: T
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD

3-167413475-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413475
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413475
    reference: chr 3
allele count: 1
allele frequency: 8.237639422047218e-6
allele num: 121394
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.1028G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.304G>A
  hgvsp: ENSP00000420424.2:p.Asp102Asn
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.304G>A
  hgvsp: ENSP00000417876.1:p.Asp102Asn
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.304G>A
  hgvsp: ENSP00000417202.1:p.Asp102Asn
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.115G>A
  hgvsp: ENSP00000417309.1:p.Asp39Asn
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.304G>A
  hgvsp: ENSP00000418317.2:p.Asp102Asn
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.304G>A
  hgvsp: ENSP00000420553.2:p.Asp102Asn
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.304G>A
  hgvsp: ENSP00000376506.2:p.Asp102Asn
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.304G>A
  hgvsp: ENSP00000417118.2:p.Asp102Asn
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.304G>A
  hgvsp: ENSP00000420021.1:p.Asp102Asn
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.304G>A
  hgvsp: ENSP00000420266.2:p.Asp102Asn
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.304G>A
  hgvsp: ENSP00000420014.1:p.Asp102Asn
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*252G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.245G>A
  hgvsp: ENSP00000420308.1:p.Asp83Asn
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9017
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1545
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5772
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp102Asn
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS

3-167413495-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413495
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413495
    reference: chr 3
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.284G>A
  hgvsp: ENSP00000420553.2:p.Arg95Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.284G>A
  hgvsp: ENSP00000417202.1:p.Arg95Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.284G>A
  hgvsp: ENSP00000420424.2:p.Arg95Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.284G>A
  hgvsp: ENSP00000420014.1:p.Arg95Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.284G>A
  hgvsp: ENSP00000417876.1:p.Arg95Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.95G>A
  hgvsp: ENSP00000417309.1:p.Arg32Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*232G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.284G>A
  hgvsp: ENSP00000376506.2:p.Arg95Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.284G>A
  hgvsp: ENSP00000420266.2:p.Arg95Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.225G>A
  hgvsp: ENSP00000420308.1:p.Arg76Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.284G>A
  hgvsp: ENSP00000420021.1:p.Arg95Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.284G>A
  hgvsp: ENSP00000417118.2:p.Arg95Gln
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.1008G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.284G>A
  hgvsp: ENSP00000418317.2:p.Arg95Gln
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1189
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1906
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg95Gln
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

3-167413497-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413497
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413497
    reference: chr 3
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.282A>G
  hgvsp: ENST00000470131.1:c.282A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.282A>G
  hgvsp: ENST00000473645.2:c.282A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.1006A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.282A>G
  hgvsp: ENST00000461494.1:c.282A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.223A>G
  hgvsp: ENST00000479121.1:c.223A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.282A>G
  hgvsp: ENST00000487947.2:c.282A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.282A>G
  hgvsp: ENST00000492139.1:c.282A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.282A>G
  hgvsp: ENST00000475915.2:c.282A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.282A>G
  hgvsp: ENST00000392750.2:c.282A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.93A>G
  hgvsp: ENST00000492396.1:c.93A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.282A>G
  hgvsp: ENST00000497056.2:c.282A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.282A>G
  hgvsp: ENST00000462725.2:c.282A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.282A>G
  hgvsp: ENST00000471885.1:c.282A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*230A>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10459
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8508
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu94Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

3-167413505-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413505
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413505
    reference: chr 3
allele count: 5
allele frequency: 4.120381052839767e-5
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.215A>G
  hgvsp: ENSP00000420308.1:p.Met73Val
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.274A>G
  hgvsp: ENSP00000376506.2:p.Met92Val
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.85A>G
  hgvsp: ENSP00000417309.1:p.Met29Val
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.274A>G
  hgvsp: ENSP00000420014.1:p.Met92Val
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.274A>G
  hgvsp: ENSP00000420266.2:p.Met92Val
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.998A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.274A>G
  hgvsp: ENSP00000417118.2:p.Met92Val
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.274A>G
  hgvsp: ENSP00000418317.2:p.Met92Val
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.274A>G
  hgvsp: ENSP00000417202.1:p.Met92Val
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.274A>G
  hgvsp: ENSP00000420021.1:p.Met92Val
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.274A>G
  hgvsp: ENSP00000417876.1:p.Met92Val
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.274A>G
  hgvsp: ENSP00000420424.2:p.Met92Val
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*222A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.274A>G
  hgvsp: ENSP00000420553.2:p.Met92Val
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7489
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10454
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8496
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2955
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met92Val
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: DP

3-167413507-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413507
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413507
    reference: chr 3
allele count: 1
allele frequency: 8.240354664864776e-6
allele num: 121354
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.83A>G
  hgvsp: ENSP00000417309.1:p.Tyr28Cys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.272A>G
  hgvsp: ENSP00000420553.2:p.Tyr91Cys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.272A>G
  hgvsp: ENSP00000417202.1:p.Tyr91Cys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.272A>G
  hgvsp: ENSP00000420021.1:p.Tyr91Cys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.272A>G
  hgvsp: ENSP00000420014.1:p.Tyr91Cys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.996A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.272A>G
  hgvsp: ENSP00000376506.2:p.Tyr91Cys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*220A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.213A>G
  hgvsp: ENSP00000420308.1:p.Tyr72Cys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.272A>G
  hgvsp: ENSP00000417118.2:p.Tyr91Cys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.272A>G
  hgvsp: ENSP00000418317.2:p.Tyr91Cys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.272A>G
  hgvsp: ENSP00000420266.2:p.Tyr91Cys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.272A>G
  hgvsp: ENSP00000417876.1:p.Tyr91Cys
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.272A>G
  hgvsp: ENSP00000420424.2:p.Tyr91Cys
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10456
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5766
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2893
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Tyr91Cys
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum

3-167413515-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413515
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413515
    reference: chr 3
allele count: 2
allele frequency: 1.648614339647526e-5
allele num: 121314
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.269-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.269-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.993-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.269-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*217-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.269-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.210-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.269-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.269-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.269-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.269-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.269-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.80-5A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.269-5A>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2957
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2161
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.269-5A>G
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum

3-167413518-AATAAATAC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413518
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413510
    reference: chr 3
allele count: 1
allele frequency: 8.244023083264634e-6
allele num: 121300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.269-16_269-9delGTATTTAT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.269-16_269-9delGTATTTAT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.269-16_269-9delGTATTTAT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.269-16_269-9delGTATTTAT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.269-16_269-9delGTATTTAT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.993-16_993-9delGTATTTAT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.269-16_269-9delGTATTTAT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*217-16_*217-9delGTATTTAT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.269-16_269-9delGTATTTAT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.210-16_210-9delGTATTTAT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.80-16_80-9delGTATTTAT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.269-16_269-9delGTATTTAT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.269-16_269-9delGTATTTAT
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.269-16_269-9delGTATTTAT
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 1829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8473
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2162
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: AATAAATAC
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD

3-167413526-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413526
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413526
    reference: chr 3
allele count: 6
allele frequency: 4.949514947535141e-5
allele num: 121224
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*217-16G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.269-16G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.210-16G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.269-16G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.269-16G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.269-16G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.269-16G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.269-16G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.269-16G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.269-16G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.269-16G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.269-16G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.80-16G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.993-16G>A
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1779
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2954
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2164
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7481
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10393
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5756
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
population: South Asian
reference allele: C
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

3-167413532-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413532
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413532
    reference: chr 3
allele count: 1
allele frequency: 8.252731654177533e-6
allele num: 121172
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.269-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.269-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.269-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.269-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.269-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.269-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.80-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.993-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.210-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*217-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.269-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.269-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.269-22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.269-22T>C
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8981
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5755
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1542
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10328
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8322
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7474
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

3-167413539-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413539
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413539
    reference: chr 3
allele count: 1
allele frequency: 8.259002312520648e-6
allele num: 121080
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.80-29T>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.269-29T>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.269-29T>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.269-29T>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.269-29T>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.269-29T>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.210-29T>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.269-29T>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.993-29T>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.269-29T>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.269-29T>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*217-29T>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.269-29T>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.269-29T>A
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 610
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8050
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10085
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5753
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4185
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP

3-167413540-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413540
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413540
    reference: chr 3
allele count: 82
allele frequency: 6.77450802200889e-4
allele num: 121042
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.80-30A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.269-30A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.269-30A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.269-30A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.269-30A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.269-30A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.269-30A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.269-30A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.993-30A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*217-30A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.269-30A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.269-30A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.269-30A>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.210-30A>T
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 743
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9998
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 9.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 7434
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8807
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 460
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7986
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4183
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/3-167413545-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413545
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413545
    reference: chr 3
allele count: 1
allele frequency: 8.270888127967181e-6
allele num: 120906
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.269-35G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.269-35G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.269-35G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.269-35G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.80-35G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.269-35G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.993-35G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.210-35G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*217-35G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.269-35G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.269-35G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.269-35G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.269-35G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.269-35G>T
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7337
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5721
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

3-167413545-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413545
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413545
    reference: chr 3
allele count: 1
allele frequency: 8.270888127967181e-6
allele num: 120906
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.269-35G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.269-35G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.80-35G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.269-35G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.269-35G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.269-35G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.269-35G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*217-35G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.269-35G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.269-35G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.269-35G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.210-35G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.269-35G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.993-35G>A
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8510
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2948
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9511
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

3-167413546-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413546
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413546
    reference: chr 3
allele count: 4
allele frequency: 3.309340613882684e-5
allele num: 120870
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.993-36C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.269-36C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.269-36C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.269-36C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.269-36C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.269-36C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.269-36C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.269-36C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.80-36C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*217-36C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.269-36C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.210-36C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.269-36C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.269-36C>T
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5719
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1541
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9460
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1321
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8035
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff

3-167413547-ACT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413547
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413545
    reference: chr 3
allele count: 4
allele frequency: 3.309285856112251e-5
allele num: 120872
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.269-39_269-38delAG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.269-39_269-38delAG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*217-39_*217-38delAG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.269-39_269-38delAG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.210-39_210-38delAG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.269-39_269-38delAG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.269-39_269-38delAG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.269-39_269-38delAG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.993-39_993-38delAG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.80-39_80-38delAG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.269-39_269-38delAG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.269-39_269-38delAG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.269-39_269-38delAG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.269-39_269-38delAG
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8480
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2946
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4169
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7878
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: ACT
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ

3-167413550-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413550
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413550
    reference: chr 3
allele count: 1
allele frequency: 8.275268532463878e-6
allele num: 120842
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.269-40G>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.269-40G>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.993-40G>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.269-40G>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.269-40G>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.210-40G>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*217-40G>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.269-40G>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.80-40G>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.269-40G>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.269-40G>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.269-40G>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.269-40G>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.269-40G>C
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9224
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2233
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 915
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5706
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1675
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2945
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1540
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4169
  bin: 5.25e1
  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: C
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

http://identifiers.org/exac.variant/3-167413555-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413555
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413555
    reference: chr 3
allele count: 1
allele frequency: 8.284455048546906e-6
allele num: 120708
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*217-45G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.210-45G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.269-45G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.993-45G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.269-45G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.269-45G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.269-45G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.269-45G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.269-45G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.269-45G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.269-45G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.80-45G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.269-45G>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.269-45G>T
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5697
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2151
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3316
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS

3-167413562-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167413562
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167413562
    reference: chr 3
allele count: 1
allele frequency: 8.294900295298451e-6
allele num: 120556
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.269-52G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.269-52G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.993-52G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.269-52G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.269-52G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.80-52G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.210-52G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.269-52G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*217-52G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.269-52G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.269-52G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.269-52G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.269-52G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.269-52G>A
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8280
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4164
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2944
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6812
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5691
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7263
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/3-167414746-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167414746
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167414746
    reference: chr 3
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.268+51T>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.268+51T>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.268+51T>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.268+51T>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.268+51T>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*216+51T>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.992+51T>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.268+51T>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.268+51T>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.209+51T>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.268+51T>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.268+51T>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.268+51T>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.79+51T>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: A
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

3-167414746-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167414746
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167414746
    reference: chr 3
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.268+51T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.268+51T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.268+51T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.992+51T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.268+51T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.268+51T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.268+51T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*216+51T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.268+51T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.268+51T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.79+51T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.209+51T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.268+51T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.268+51T>C
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24034
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7867
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4621
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 696
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: MQ

3-167414751-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167414751
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167414751
    reference: chr 3
allele count: 1
allele frequency: 8.241712957621112e-6
allele num: 121334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*216+46G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.268+46G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.268+46G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.268+46G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.209+46G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.992+46G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.268+46G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.268+46G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.268+46G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.268+46G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.268+46G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.79+46G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.268+46G>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.268+46G>A
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7946
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24039
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11635
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4624
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

3-167414755-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167414755
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167414755
    reference: chr 3
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.79+42A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*216+42A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.268+42A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.992+42A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.268+42A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.268+42A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.268+42A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.268+42A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.209+42A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.268+42A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.268+42A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.268+42A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.268+42A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.268+42A>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7996
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

3-167414762-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167414762
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167414762
    reference: chr 3
allele count: 15
allele frequency: 1.23611431585193e-4
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.268+35A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.268+35A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.268+35A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.268+35A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.268+35A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.268+35A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*216+35A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.268+35A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.268+35A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.209+35A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.992+35A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.268+35A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.268+35A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.79+35A>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1762
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8057
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 4.25e1
  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: T
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP

3-167414764-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167414764
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167414764
    reference: chr 3
allele count: 11
allele frequency: 9.064688916357643e-5
allele num: 121350
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.268+33C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.268+33C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.268+33C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*216+33C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.268+33C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.79+33C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.268+33C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.268+33C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.268+33C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.209+33C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.992+33C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.268+33C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.268+33C>A
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.268+33C>A
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2618
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8065
  bin: 2.25e1
  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: South Asian
population: Other
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

3-167414765-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167414765
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167414765
    reference: chr 3
allele count: 2
allele frequency: 1.648152421135907e-5
allele num: 121348
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.992+32A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.268+32A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.209+32A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.268+32A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*216+32A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.268+32A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.268+32A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.79+32A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.268+32A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.268+32A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.268+32A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.268+32A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.268+32A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.268+32A>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1494
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24083
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

3-167414772-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167414772
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167414772
    reference: chr 3
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.209+25A>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.992+25A>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.268+25A>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.268+25A>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.268+25A>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.268+25A>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.268+25A>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*216+25A>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.268+25A>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.268+25A>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.268+25A>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.79+25A>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.268+25A>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.268+25A>C
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24092
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 892
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1055
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8109
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: DP

3-167414775-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167414775
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167414775
    reference: chr 3
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.268+22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.268+22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.268+22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.268+22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.268+22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.268+22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.268+22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.209+22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*216+22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.268+22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.79+22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.268+22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.992+22T>C
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.268+22T>C
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11644
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP

3-167414775-ACAAGGTT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167414775
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167414768
    reference: chr 3
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.268+15_268+21delAACCTTG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.268+15_268+21delAACCTTG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.268+15_268+21delAACCTTG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.268+15_268+21delAACCTTG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.268+15_268+21delAACCTTG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*216+15_*216+21delAACCTTG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.268+15_268+21delAACCTTG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.268+15_268+21delAACCTTG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.79+15_79+21delAACCTTG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.209+15_209+21delAACCTTG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.268+15_268+21delAACCTTG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.268+15_268+21delAACCTTG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.268+15_268+21delAACCTTG
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.992+15_992+21delAACCTTG
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24096
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 893
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4616
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: ACAAGGTT
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum

3-167414779-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167414779
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167414779
    reference: chr 3
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.79+18C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*216+18C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.268+18C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.209+18C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.268+18C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.268+18C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.268+18C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.268+18C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.268+18C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.268+18C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.268+18C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.268+18C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.268+18C>T
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.992+18C>T
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8127
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11651
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24101
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

3-167414789-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 167414789
    reference: chr 3
  end: Position
    type: ExactPosition
    position: 167414789
    reference: chr 3
allele count: 1
allele frequency: 8.239811473113496e-6
allele num: 121362
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420450
  ensembl transcript: ENST00000494502
  gene symbol: PDCD10
  hgvsc: ENST00000494502.2:c.*216+8A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417118
  ensembl transcript: ENST00000475915
  gene symbol: PDCD10
  hgvsc: ENST00000475915.2:c.268+8A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420308
  ensembl transcript: ENST00000479121
  gene symbol: PDCD10
  hgvsc: ENST00000479121.1:c.209+8A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417202
  ensembl transcript: ENST00000470131
  gene symbol: PDCD10
  hgvsc: ENST00000470131.1:c.268+8A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420021
  ensembl transcript: ENST00000461494
  gene symbol: PDCD10
  hgvsc: ENST00000461494.1:c.268+8A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420266
  ensembl transcript: ENST00000487947
  gene symbol: PDCD10
  hgvsc: ENST00000487947.2:c.268+8A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000418317
  ensembl transcript: ENST00000473645
  gene symbol: PDCD10
  hgvsc: ENST00000473645.2:c.268+8A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420014
  ensembl transcript: ENST00000492139
  gene symbol: PDCD10
  hgvsc: ENST00000492139.1:c.268+8A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420424
  ensembl transcript: ENST00000462725
  gene symbol: PDCD10
  hgvsc: ENST00000462725.2:c.268+8A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl transcript: ENST00000483451
  gene symbol: PDCD10
  hgvsc: ENST00000483451.1:n.992+8A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417876
  ensembl transcript: ENST00000471885
  gene symbol: PDCD10
  hgvsc: ENST00000471885.1:c.268+8A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000420553
  ensembl transcript: ENST00000497056
  gene symbol: PDCD10
  hgvsc: ENST00000497056.2:c.268+8A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000376506
  ensembl transcript: ENST00000392750
  gene symbol: PDCD10
  hgvsc: ENST00000392750.2:c.268+8A>G
  variant of: http://identifiers.org/hgnc/8761
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000114209
  ensembl protein: ENSP00000417309
  ensembl transcript: ENST00000492396
  gene symbol: PDCD10
  hgvsc: ENST00000492396.1:c.79+8A>G
  variant of: http://identifiers.org/hgnc/8761
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11650
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1166
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1056
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1493
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1763
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.268+8A>G
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: T

GenotypeQuality
all individuals: 416
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 440
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 702
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1451
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 782
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 800
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1385
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36732
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6506
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 765
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65182
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.179523472517103e-4
allele num: 8478
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16284
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6528
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11188
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.155e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.129e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.46e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.573e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.23e-2

QD
type: SiteQuality
SIO_000300: 1.199e1

DP
type: SiteQuality
SIO_000300: 1.769764e6

MQ
type: SiteQuality
SIO_000300: 5.838e1

GenotypeQuality
all individuals: 958
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1231
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41410
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 316
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 296
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 440
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5056
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1367
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 751
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 404
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.117432530999271e-5
allele num: 65808
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16344
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.80126738250308e-5
allele num: 11362
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -6.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.1e-1

QD
type: SiteQuality
SIO_000300: 1.296e1

DP
type: SiteQuality
SIO_000300: 1.817749e6

FS
type: SiteQuality
SIO_000300: 4.095e0

MQ
type: SiteQuality
SIO_000300: 5.929e1

BaseQRankSum
type: SiteQuality
SIO_000300: 8.080000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-2

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

GenotypeQuality
all individuals: 100
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41987
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 799
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 258
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5070
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 963
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1359
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8566
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16348
num of homozygotes: 0

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

African
type: Population
allele count: 19
allele frequency: 1.83894696089818e-3
allele num: 10332
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11380
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65882
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

QD
type: SiteQuality
SIO_000300: 1.27e1

FS
type: SiteQuality
SIO_000300: 1.231e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.5e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.97e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

DP
type: SiteQuality
SIO_000300: 1.821431e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.29e-1

GenotypeQuality
all individuals: 401
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5091
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1357
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 633
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 953
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42486
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 84
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 208
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1203
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16382
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.513408801985592e-5
allele num: 66076
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.24e0

DP
type: SiteQuality
SIO_000300: 1.831881e6

MQRankSum
type: SiteQuality
SIO_000300: -1.051e0

FS
type: SiteQuality
SIO_000300: 5.225e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.42e-1

QD
type: SiteQuality
SIO_000300: 1.09e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.59e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.36e-1

GenotypeQuality
all individuals: 1207
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 112
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 72
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5119
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 749
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 951
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42551
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1354
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66142
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11428
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 3
allele frequency: 2.902476780185758e-4
allele num: 10336
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16400
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.835069e6

QD
type: SiteQuality
SIO_000300: 1.418e1

VQSLOD
type: SiteQuality
SIO_000300: 5.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.500000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.32e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.32e-1

GenotypeQuality
all individuals: 751
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42879
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 85
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 131
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6497
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 124
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 786
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 86
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5102
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1182
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 949
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1347
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 4.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16380
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.752541184717841e-4
allele num: 11412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66034
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
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MQRankSum
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SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.286e0

VQSLOD
type: SiteQuality
SIO_000300: -5.686e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

InbreedingCoeff
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SIO_000300: 1.42e-2

DP
type: SiteQuality
SIO_000300: 1.834415e6

FS
type: SiteQuality
SIO_000300: 2.497e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.28e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.57e-1

QD
type: SiteQuality
SIO_000300: 2.077e1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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variant carriers: 0

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

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515840533575868e-5
allele num: 65970
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6576
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 8.04e-1

FS
type: SiteQuality
SIO_000300: 3.586e0

ClippingRankSum
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InbreedingCoeff
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QD
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SIO_000300: 1.075e1

ReadPosRankSum
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SIO_000300: 1.08e0

MQRankSum
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SIO_000300: -2.8e-1

BaseQRankSum
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SIO_000300: 4.02e-1

MQ
type: SiteQuality
SIO_000300: 5.905e1

DP
type: SiteQuality
SIO_000300: 1.83337e6

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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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 5.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11400
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10292
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65932
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 6.111722283339445e-5
allele num: 16362
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.026e0

ClippingRankSum
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SIO_000300: -1.01e-1

ReadPosRankSum
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SIO_000300: -6.64e-1

InbreedingCoeff
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SIO_000300: -3.0e-4

DP
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SIO_000300: 1.832511e6

VQSLOD
type: SiteQuality
SIO_000300: 4.8e-1

QD
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SIO_000300: 1.516e1

BaseQRankSum
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SIO_000300: 9.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.6e-2

MQ
type: SiteQuality
SIO_000300: 5.978e1

GenotypeDepth
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 1140
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10172
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6544
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11284
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65216
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8520
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 884
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.154603643525357e-5
allele num: 16248
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.42e-1

DP
type: SiteQuality
SIO_000300: 1.814239e6

MQ
type: SiteQuality
SIO_000300: 5.945e1

QD
type: SiteQuality
SIO_000300: 1.319e1

MQRankSum
type: SiteQuality
SIO_000300: 5.35e-1

VQSLOD
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SIO_000300: 4.87e-1

FS
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SIO_000300: 0.0e0

BaseQRankSum
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SIO_000300: 3.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -3.97e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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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: 9.75e1
variant carriers: 4

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9856
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.514458134272064e-4
allele num: 15908
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 62764
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15814
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.836210062431142e-4
allele num: 10892
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

African
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allele count: 0
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allele num: 9400
num of homozygotes: 0

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

Latino
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allele num: 10436
num of homozygotes: 0

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

Other
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South Asian
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allele num: 15488
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European (Non-Finnish)
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InbreedingCoeff
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QD
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BaseQRankSum
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FS
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DP
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MQRankSum
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ClippingRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10424
num of homozygotes: 0

Other
type: Population
allele count: 0
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African
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East Asian
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.694915254237288e-5
allele num: 59000
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European (Finnish)
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

FS
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SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.91e-1

MQ
type: SiteQuality
SIO_000300: 5.54e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.437e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.84e0

QD
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
SIO_000300: 1.531013e6

GenotypeQuality
all individuals: 12947
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2663
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 20181
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GenotypeQuality
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variant carriers: 114

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
all individuals: 5158
bin: 3.25e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2812
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.779661016949152e-5
allele num: 59000
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.290322580645161e-4
allele num: 7750
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6280
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.409638554216868e-3
allele num: 830
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10424
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9364
num of homozygotes: 0

South Asian
type: Population
allele count: 105
allele frequency: 6.783822199250549e-3
allele num: 15478
num of homozygotes: 2

QD
type: SiteQuality
SIO_000300: 1.2e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.31e-1

DP
type: SiteQuality
SIO_000300: 1.531013e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.11e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.04e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.437e-1

MQ
type: SiteQuality
SIO_000300: 5.54e1

MQRankSum
type: SiteQuality
SIO_000300: -2.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.91e-1

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 492
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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
all individuals: 677
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variant carriers: 0

GenotypeQuality
all individuals: 971
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7560
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9186
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.730283420424266e-5
allele num: 57794
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6242
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.615506747816882e-5
allele num: 15116
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 812
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.44705e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.67e0

MQRankSum
type: SiteQuality
SIO_000300: -7.44e-1

FS
type: SiteQuality
SIO_000300: 1.266e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

MQ
type: SiteQuality
SIO_000300: 5.964e1

VQSLOD
type: SiteQuality
SIO_000300: -3.125e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

QD
type: SiteQuality
SIO_000300: 1.255e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.25e-1

GenotypeDepth
all individuals: 1098
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variant carriers: 0

GenotypeQuality
all individuals: 90
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GenotypeQuality
all individuals: 549
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 11193
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GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
all individuals: 650
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variant carriers: 0

GenotypeQuality
all individuals: 930
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.750393838613688e-5
allele num: 57130
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15042
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9080
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7464
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.22e1

MQRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.02e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.369e0

DP
type: SiteQuality
SIO_000300: 1.414194e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.473e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.95e0

GenotypeDepth
all individuals: 242
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variant carriers: 0

GenotypeQuality
all individuals: 1886
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variant carriers: 0

GenotypeQuality
all individuals: 926
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variant carriers: 0

GenotypeQuality
all individuals: 5855
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variant carriers: 0

GenotypeQuality
all individuals: 1767
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variant carriers: 0

GenotypeQuality
all individuals: 684
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variant carriers: 0

GenotypeQuality
all individuals: 12986
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variant carriers: 0

GenotypeQuality
all individuals: 1994
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GenotypeQuality
all individuals: 8041
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GenotypeQuality
all individuals: 742
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6440
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GenotypeQuality
all individuals: 727
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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14982
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 804
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8982
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7358
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6206
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.875567845151097e-5
allele num: 10126
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56576
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.199e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.39e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.571e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.33e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.782e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

QD
type: SiteQuality
SIO_000300: 1.117e1

MQ
type: SiteQuality
SIO_000300: 5.991e1

DP
type: SiteQuality
SIO_000300: 1.39465e6

GenotypeDepth
all individuals: 545
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variant carriers: 0

GenotypeQuality
all individuals: 1319
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2665
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 6440
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GenotypeQuality
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GenotypeQuality
all individuals: 8324
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GenotypeQuality
all individuals: 5271
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GenotypeQuality
all individuals: 907
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7146
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.823420006564312e-5
allele num: 54842
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14764
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6144
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9906
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.69e0

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -5.02e-1

ReadPosRankSum
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DP
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.619e1

InbreedingCoeff
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SIO_000300: -2.5e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.936e1

VQSLOD
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SIO_000300: 2.94e0

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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variant carriers: 41

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6660
bin: 3.75e1
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GenotypeQuality
all individuals: 576
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 7.509557618787547e-4
allele num: 14648
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7010
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.644195988161789e-4
allele num: 6082
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.152604887044721e-4
allele num: 8676
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 27
allele frequency: 5.040322580645161e-4
allele num: 53568
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.348951e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

QD
type: SiteQuality
SIO_000300: 1.413e1

BaseQRankSum
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SIO_000300: -2.464e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.12e0

GenotypeDepth
all individuals: 129
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variant carriers: 0

GenotypeQuality
all individuals: 3949
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 790
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variant carriers: 0

GenotypeQuality
all individuals: 6473
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.733572281959379e-5
allele num: 53568
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8676
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 790
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7010
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9712
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6082
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14648
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.348951e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
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SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.12e0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

African
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allele count: 1
allele frequency: 9.626492106276473e-5
allele num: 10388
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

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

VQSLOD
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MQRankSum
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FS
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SIO_000300: 5.518e0

ReadPosRankSum
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MQ
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SIO_000300: 5.99e1

ClippingRankSum
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SIO_000300: 6.31e-1

DP
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SIO_000300: 2.841485e6

QD
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SIO_000300: 1.408e1

BaseQRankSum
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SIO_000300: -9.01e-1

InbreedingCoeff
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SIO_000300: 7.900000000000001e-3

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 4157
bin: 7.75e1
variant carriers: 0

African
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allele count: 1
allele frequency: 9.628345850182938e-5
allele num: 10386
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8648
num of homozygotes: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498935755613514e-5
allele num: 66714
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.841787e6

ClippingRankSum
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SIO_000300: -1.288e0

InbreedingCoeff
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SIO_000300: 4.9e-3

ReadPosRankSum
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MQ
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SIO_000300: 6.0e1

VQSLOD
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SIO_000300: 3.28e0

FS
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: 1.24e-1

QD
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SIO_000300: 1.282e1

BaseQRankSum
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SIO_000300: -3.821e0

GenotypeDepth
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variant carriers: 35

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 355

GenotypeQuality
all individuals: 50
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 309
allele frequency: 4.631294964028777e-3
allele num: 66720
num of homozygotes: 0

Other
type: Population
allele count: 4
allele frequency: 4.415011037527594e-3
allele num: 906
num of homozygotes: 0

South Asian
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allele count: 2
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allele num: 16510
num of homozygotes: 0

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

European (Finnish)
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allele count: 31
allele frequency: 4.688445251058681e-3
allele num: 6612
num of homozygotes: 1

African
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allele count: 2
allele frequency: 1.926040061633282e-4
allele num: 10384
num of homozygotes: 0

Latino
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allele frequency: 6.912044237083118e-4
allele num: 11574
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 9.71e-1

ReadPosRankSum
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SIO_000300: 7.4e-1

MQRankSum
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VQSLOD
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MQ
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SIO_000300: 5.974e1

InbreedingCoeff
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SIO_000300: 5.0e-4

ClippingRankSum
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SIO_000300: -2.48e-1

BaseQRankSum
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SIO_000300: 4.57e0

QD
type: SiteQuality
SIO_000300: 1.41e1

DP
type: SiteQuality
SIO_000300: 2.843898e6

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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 9181
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GenotypeQuality
all individuals: 2533
bin: 7.25e1
variant carriers: 0

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.374e-1

InbreedingCoeff
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SIO_000300: -4.0e-4

MQ
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SIO_000300: 5.915e1

ReadPosRankSum
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SIO_000300: 2.18e0

DP
type: SiteQuality
SIO_000300: 2.834663e6

MQRankSum
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SIO_000300: 7.38e-1

FS
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SIO_000300: 2.488e0

QD
type: SiteQuality
SIO_000300: 1.054e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.99e-1

BaseQRankSum
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SIO_000300: -9.64e-1

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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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.25e1
variant carriers: 0

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

African
type: Population
allele count: 4
allele frequency: 3.848374061958822e-4
allele num: 10394
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

ClippingRankSum
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QD
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VQSLOD
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FS
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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DP
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SIO_000300: 2.834825e6

MQ
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SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.05e-1

InbreedingCoeff
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SIO_000300: -3.0e-4

GenotypeDepth
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variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 5260
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GenotypeQuality
all individuals: 3640
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66728
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 1.155802126675913e-4
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num of homozygotes: 0

South Asian
type: Population
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African
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allele frequency: 1.923816852635629e-4
allele num: 10396
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DP
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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MQRankSum
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FS
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MQ
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InbreedingCoeff
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QD
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BaseQRankSum
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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European (Non-Finnish)
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East Asian
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South Asian
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MQ
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QD
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BaseQRankSum
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DP
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InbreedingCoeff
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FS
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MQRankSum
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VQSLOD
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ReadPosRankSum
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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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South Asian
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African
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European (Non-Finnish)
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European (Finnish)
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Other
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East Asian
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FS
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InbreedingCoeff
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MQ
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DP
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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East Asian
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South Asian
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African
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VQSLOD
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ReadPosRankSum
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MQRankSum
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InbreedingCoeff
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FS
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ClippingRankSum
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BaseQRankSum
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DP
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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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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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African
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Latino
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East Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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South Asian
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ReadPosRankSum
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QD
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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FS
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MQ
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MQRankSum
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DP
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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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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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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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South Asian
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East Asian
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Other
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VQSLOD
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FS
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ClippingRankSum
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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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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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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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European (Finnish)
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African
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Latino
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East Asian
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South Asian
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European (Non-Finnish)
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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FS
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VQSLOD
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MQRankSum
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DP
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele frequency: 4.495594317568783e-5
allele num: 66732
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

South Asian
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num of homozygotes: 0

Other
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num of homozygotes: 0

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

Latino
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allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

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

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

East Asian
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Other
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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

MQ
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ReadPosRankSum
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VQSLOD
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QD
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FS
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DP
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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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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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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variant carriers: 5

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997062878379188e-5
allele num: 66732
num of homozygotes: 0

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

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

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

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

Latino
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allele frequency: 2.591568762957844e-4
allele num: 11576
num of homozygotes: 0

VQSLOD
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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ReadPosRankSum
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SIO_000300: 1.6e-1

FS
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SIO_000300: 1.143e0

MQ
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SIO_000300: 5.941e1

QD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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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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East Asian
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allele count: 0
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num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.640055296353897e-5
allele num: 11574
num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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European (Finnish)
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South Asian
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Other
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ReadPosRankSum
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VQSLOD
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MQRankSum
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MQ
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QD
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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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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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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African
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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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South Asian
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Other
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VQSLOD
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ReadPosRankSum
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MQ
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MQRankSum
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DP
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FS
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InbreedingCoeff
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QD
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ClippingRankSum
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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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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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South Asian
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Other
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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MQRankSum
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MQ
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VQSLOD
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ReadPosRankSum
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DP
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FS
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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South Asian
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allele frequency: 3.028467595396729e-4
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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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num of homozygotes: 0

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

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

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

East Asian
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allele frequency: 0.0e0
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South Asian
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allele num: 16510
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Latino
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African
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ReadPosRankSum
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VQSLOD
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InbreedingCoeff
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DP
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MQRankSum
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ClippingRankSum
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FS
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MQ
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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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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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South Asian
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African
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allele frequency: 0.0e0
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Latino
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European (Finnish)
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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MQRankSum
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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DP
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InbreedingCoeff
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MQ
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FS
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VQSLOD
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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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European (Non-Finnish)
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Latino
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European (Finnish)
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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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FS
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQ
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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South Asian
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European (Non-Finnish)
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Other
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Latino
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European (Finnish)
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African
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BaseQRankSum
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DP
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QD
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VQSLOD
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MQRankSum
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FS
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ReadPosRankSum
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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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East Asian
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num of homozygotes: 0

European (Non-Finnish)
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South Asian
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European (Finnish)
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Other
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African
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Latino
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InbreedingCoeff
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BaseQRankSum
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MQ
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 3.427e0

ClippingRankSum
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SIO_000300: 1.19e0

MQRankSum
type: SiteQuality
SIO_000300: -7.22e-1

QD
type: SiteQuality
SIO_000300: 1.16e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.07e-1

DP
type: SiteQuality
SIO_000300: 2.813651e6

GenotypeDepth
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bin: 7.25e1
variant carriers: 7

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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bin: 4.75e1
variant carriers: 4

GenotypeDepth
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bin: 5.75e1
variant carriers: 8

GenotypeDepth
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variant carriers: 3

GenotypeQuality
all individuals: 4131
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 81

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7904
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4069
bin: 8.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10216
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.500915558490679e-5
allele num: 66626
num of homozygotes: 0

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

South Asian
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allele count: 81
allele frequency: 4.906711897261933e-3
allele num: 16508
num of homozygotes: 1

MQRankSum
type: SiteQuality
SIO_000300: 1.37e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

VQSLOD
type: SiteQuality
SIO_000300: 2.37e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

FS
type: SiteQuality
SIO_000300: 1.775e0

BaseQRankSum
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SIO_000300: -2.223e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.3e-2

DP
type: SiteQuality
SIO_000300: 2.812318e6

QD
type: SiteQuality
SIO_000300: 1.238e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-2

GenotypeDepth
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bin: 7.5e0
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.875567845151097e-5
allele num: 10126
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 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: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66588
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.28e0

FS
type: SiteQuality
SIO_000300: 9.949e0

DP
type: SiteQuality
SIO_000300: 2.793316e6

VQSLOD
type: SiteQuality
SIO_000300: 3.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.78e-1

QD
type: SiteQuality
SIO_000300: 1.502e1

MQRankSum
type: SiteQuality
SIO_000300: 7.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4037
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.875567845151097e-5
allele num: 10126
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66588
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.502e1

VQSLOD
type: SiteQuality
SIO_000300: 3.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.78e-1

DP
type: SiteQuality
SIO_000300: 2.793316e6

FS
type: SiteQuality
SIO_000300: 9.949e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.8e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.91e-1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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variant carriers: 4

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.817520901490367e-4
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11546
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502268425322237e-5
allele num: 66566
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10120
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 7.46e-1

DP
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SIO_000300: 2.79235e6

MQ
type: SiteQuality
SIO_000300: 5.974e1

FS
type: SiteQuality
SIO_000300: 6.29e-1

ReadPosRankSum
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QD
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ClippingRankSum
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SIO_000300: 8.72e-1

BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 6.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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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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variant carriers: 4

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

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.506263706552107e-5
allele num: 66574
num of homozygotes: 0

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

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

South Asian
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allele frequency: 6.05913717886573e-5
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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InbreedingCoeff
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ReadPosRankSum
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.236e0

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

QD
type: SiteQuality
SIO_000300: 1.668e1

MQ
type: SiteQuality
SIO_000300: 5.972e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 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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variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10104
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66554
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11548
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.785113e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 1.199e0

VQSLOD
type: SiteQuality
SIO_000300: 2.15e-1

MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.518e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.99e0

QD
type: SiteQuality
SIO_000300: 1.651e1

GenotypeDepth
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bin: 2.75e1
variant carriers: 0

GenotypeDepth
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bin: 9.25e1
variant carriers: 0

GenotypeDepth
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bin: 6.75e1
variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 291
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.503578516870151e-5
allele num: 66508
num of homozygotes: 0

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

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

InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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DP
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QD
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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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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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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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allele frequency: 0.0e0
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African
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East Asian
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European (Non-Finnish)
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allele frequency: 1.504573904670197e-5
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VQSLOD
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MQ
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ReadPosRankSum
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DP
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MQRankSum
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FS
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QD
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InbreedingCoeff
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ClippingRankSum
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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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variant carriers: 0

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

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11566
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

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

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

European (Finnish)
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East Asian
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African
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South Asian
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European (Non-Finnish)
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allele num: 66702
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Latino
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MQ
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FS
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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MQRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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South Asian
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African
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European (Finnish)
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Other
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East Asian
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FS
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VQSLOD
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QD
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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DP
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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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Latino
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num of homozygotes: 0

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

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

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: 1.057285659361784e-3
allele num: 10404
num of homozygotes: 0

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

Other
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allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

Latino
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num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 1.49902563333833e-5
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num of homozygotes: 0

FS
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MQRankSum
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ReadPosRankSum
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BaseQRankSum
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MQ
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QD
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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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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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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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

Latino
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num of homozygotes: 0

African
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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ClippingRankSum
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QD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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VQSLOD
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BaseQRankSum
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FS
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MQ
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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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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

European (Non-Finnish)
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Other
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African
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East Asian
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South Asian
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Latino
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InbreedingCoeff
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QD
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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FS
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MQRankSum
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VQSLOD
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MQ
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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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East Asian
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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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European (Finnish)
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MQ
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DP
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VQSLOD
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FS
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InbreedingCoeff
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QD
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ReadPosRankSum
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ClippingRankSum
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MQRankSum
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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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South Asian
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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InbreedingCoeff
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VQSLOD
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QD
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BaseQRankSum
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DP
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FS
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MQRankSum
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MQ
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ClippingRankSum
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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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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1722
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11734
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4069
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 8011
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27959
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2969
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1255
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0