10-103340020-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340020
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340020
    reference: chr 10
allele count: 1
allele frequency: 8.339588024351597e-6
allele num: 119910
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1963A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1348A>G
  hgvsp: ENSP00000299206.4:p.Ser450Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1348A>G
  hgvsp: ENSP00000359181.3:p.Ser450Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.517A>G
  hgvsp: ENSP00000406791.1:p.Ser173Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.367A>G
  hgvsp: ENSP00000359187.3:p.Ser123Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1084A>G
  hgvsp: ENSP00000359191.1:p.Ser362Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1072A>G
  hgvsp: ENSP00000400676.1:p.Ser358Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.394T>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1348A>G
  hgvsp: ENSP00000359188.1:p.Ser450Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.523A>G
  hgvsp: ENSP00000359177.3:p.Ser175Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.777A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.559A>G
  hgvsp: ENSP00000390810.2:p.Ser187Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.517A>G
  hgvsp: ENSP00000343102.3:p.Ser173Gly
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.618A>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-222T>C
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9761
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9453
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser450Gly
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

10-103340029-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340029
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340029
    reference: chr 10
allele count: 1
allele frequency: 8.300959590928711e-6
allele num: 120468
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.550C>T
  hgvsp: ENSP00000390810.2:p.Leu184Phe
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-213G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1075C>T
  hgvsp: ENSP00000359191.1:p.Leu359Phe
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.403G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.508C>T
  hgvsp: ENSP00000343102.3:p.Leu170Phe
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1339C>T
  hgvsp: ENSP00000359181.3:p.Leu447Phe
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1339C>T
  hgvsp: ENSP00000299206.4:p.Leu447Phe
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1954C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.508C>T
  hgvsp: ENSP00000406791.1:p.Leu170Phe
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.358C>T
  hgvsp: ENSP00000359187.3:p.Leu120Phe
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.514C>T
  hgvsp: ENSP00000359177.3:p.Leu172Phe
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1063C>T
  hgvsp: ENSP00000400676.1:p.Leu355Phe
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1339C>T
  hgvsp: ENSP00000359188.1:p.Leu447Phe
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.768C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.609C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 237
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4946
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu447Phe
num of homozygotes: 0
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP

10-103340031-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340031
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340031
    reference: chr 10
allele count: 1
allele frequency: 8.297653423611802e-6
allele num: 120516
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.548G>A
  hgvsp: ENSP00000390810.2:p.Arg183His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.356G>A
  hgvsp: ENSP00000359187.3:p.Arg119His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.506G>A
  hgvsp: ENSP00000343102.3:p.Arg169His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1061G>A
  hgvsp: ENSP00000400676.1:p.Arg354His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1337G>A
  hgvsp: ENSP00000359181.3:p.Arg446His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1337G>A
  hgvsp: ENSP00000299206.4:p.Arg446His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.506G>A
  hgvsp: ENSP00000406791.1:p.Arg169His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1952G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1337G>A
  hgvsp: ENSP00000359188.1:p.Arg446His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.766G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1073G>A
  hgvsp: ENSP00000359191.1:p.Arg358His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-211C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.405C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.512G>A
  hgvsp: ENSP00000359177.3:p.Arg171His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.607G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10019
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg446His
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum

10-103340032-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340032
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340032
    reference: chr 10
allele count: 6
allele frequency: 4.973309903517788e-5
allele num: 120644
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.505C>T
  hgvsp: ENSP00000343102.3:p.Arg169Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.511C>T
  hgvsp: ENSP00000359177.3:p.Arg171Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1336C>T
  hgvsp: ENSP00000359181.3:p.Arg446Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1060C>T
  hgvsp: ENSP00000400676.1:p.Arg354Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1336C>T
  hgvsp: ENSP00000359188.1:p.Arg446Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.765C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-210G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1951C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.505C>T
  hgvsp: ENSP00000406791.1:p.Arg169Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.355C>T
  hgvsp: ENSP00000359187.3:p.Arg119Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.547C>T
  hgvsp: ENSP00000390810.2:p.Arg183Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.406G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1336C>T
  hgvsp: ENSP00000299206.4:p.Arg446Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1072C>T
  hgvsp: ENSP00000359191.1:p.Arg358Cys
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.606C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 682
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8767
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4947
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9544
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg446Cys
num of homozygotes: 0
population: Latino
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum

10-103340036-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340036
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340036
    reference: chr 10
allele count: 3
allele frequency: 2.483032610494951e-5
allele num: 120820
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-206G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1332C>T
  hgvsp: ENST00000370169.1:c.1332C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1332C>T
  hgvsp: ENST00000299206.4:c.1332C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.501C>T
  hgvsp: ENST00000339310.3:c.501C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.507C>T
  hgvsp: ENST00000370158.3:c.507C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1332C>T
  hgvsp: ENST00000370162.3:c.1332C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1947C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1056C>T
  hgvsp: ENST00000415897.1:c.1056C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.501C>T
  hgvsp: ENST00000429502.1:c.501C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.543C>T
  hgvsp: ENST00000456836.2:c.543C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.410G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.761C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1068C>T
  hgvsp: ENST00000370172.1:c.1068C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.602C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.351C>T
  hgvsp: ENST00000370168.3:c.351C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4947
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9570
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe444Phe
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
reference allele: G
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD

10-103340041-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340041
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340040
    reference: chr 10
allele count: 1
allele frequency: 8.269520202437855e-6
allele num: 120926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.501delT
  hgvsp: ENSP00000359177.3:p.Ile168SerfsTer20
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1050delT
  hgvsp: ENSP00000400676.1:p.Ile351SerfsTer27
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1941delT
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.416delA
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1326delT
  hgvsp: ENSP00000359181.3:p.Ile443SerfsTer20
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.596delT
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.495delT
  hgvsp: ENSP00000343102.3:p.Ile166SerfsTer20
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.345delT
  hgvsp: ENSP00000359187.3:p.Ile116SerfsTer20
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1326delT
  hgvsp: ENSP00000359188.1:p.Ile443SerfsTer20
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1326delT
  hgvsp: ENSP00000299206.4:p.Ile443SerfsTer20
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1062delT
  hgvsp: ENSP00000359191.1:p.Ile355SerfsTer20
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-200delA
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.537delT
  hgvsp: ENSP00000390810.2:p.Ile180SerfsTer20
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.755delT
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.495delT
  hgvsp: ENSP00000406791.1:p.Ile166SerfsTer20
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9582
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7718
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile443SerfsTer20
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
reference allele: TA
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/10-103340042-A-AC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340042
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340043
    reference: chr 10
allele count: 1
allele frequency: 8.268426187759421e-6
allele num: 120942
alternate allele: AC
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1940dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.500dupG
  hgvsp: ENSP00000359177.3:p.Ile168TyrfsTer7
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1325dupG
  hgvsp: ENSP00000299206.4:p.Ile443TyrfsTer7
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.494dupG
  hgvsp: ENSP00000406791.1:p.Ile166TyrfsTer7
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1049dupG
  hgvsp: ENSP00000400676.1:p.Ile351TyrfsTer7
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.595dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1325dupG
  hgvsp: ENSP00000359181.3:p.Ile443TyrfsTer7
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.344dupG
  hgvsp: ENSP00000359187.3:p.Ile116TyrfsTer7
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1325dupG
  hgvsp: ENSP00000359188.1:p.Ile443TyrfsTer7
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.420dupC
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.536dupG
  hgvsp: ENSP00000390810.2:p.Ile180TyrfsTer7
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.754dupG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.494dupG
  hgvsp: ENSP00000343102.3:p.Ile166TyrfsTer7
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1061dupG
  hgvsp: ENSP00000359191.1:p.Ile355TyrfsTer7
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-196dupC
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1963
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10136
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7719
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6260
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile443TyrfsTer7
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: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

10-103340043-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340043
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340043
    reference: chr 10
allele count: 5
allele frequency: 4.133734581170012e-5
allele num: 120956
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.536G>C
  hgvsp: ENSP00000390810.2:p.Gly179Ala
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1325G>C
  hgvsp: ENSP00000299206.4:p.Gly442Ala
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.595G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.494G>C
  hgvsp: ENSP00000406791.1:p.Gly165Ala
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1325G>C
  hgvsp: ENSP00000359181.3:p.Gly442Ala
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.344G>C
  hgvsp: ENSP00000359187.3:p.Gly115Ala
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1940G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1061G>C
  hgvsp: ENSP00000359191.1:p.Gly354Ala
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.417C>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.754G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-199C>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.494G>C
  hgvsp: ENSP00000343102.3:p.Gly165Ala
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1049G>C
  hgvsp: ENSP00000400676.1:p.Gly350Ala
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.500G>C
  hgvsp: ENSP00000359177.3:p.Gly167Ala
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1325G>C
  hgvsp: ENSP00000359188.1:p.Gly442Ala
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4948
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1964
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
hgvs: p.Gly442Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

10-103340043-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340043
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340043
    reference: chr 10
allele count: 2
allele frequency: 1.653493832468005e-5
allele num: 120956
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1325G>A
  hgvsp: ENSP00000359188.1:p.Gly442Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.494G>A
  hgvsp: ENSP00000406791.1:p.Gly165Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.494G>A
  hgvsp: ENSP00000343102.3:p.Gly165Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1325G>A
  hgvsp: ENSP00000299206.4:p.Gly442Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1325G>A
  hgvsp: ENSP00000359181.3:p.Gly442Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.754G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.536G>A
  hgvsp: ENSP00000390810.2:p.Gly179Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.595G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.417C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1061G>A
  hgvsp: ENSP00000359191.1:p.Gly354Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-199C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1049G>A
  hgvsp: ENSP00000400676.1:p.Gly350Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.344G>A
  hgvsp: ENSP00000359187.3:p.Gly115Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.500G>A
  hgvsp: ENSP00000359177.3:p.Gly167Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1940G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 681
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10149
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8815
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4948
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3678
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly442Asp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: VQSLOD

10-103340044-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340044
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340044
    reference: chr 10
allele count: 1
allele frequency: 8.266239026567692e-6
allele num: 120974
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1060G>C
  hgvsp: ENSP00000359191.1:p.Gly354Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.418C>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.493G>C
  hgvsp: ENSP00000343102.3:p.Gly165Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.753G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.499G>C
  hgvsp: ENSP00000359177.3:p.Gly167Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1324G>C
  hgvsp: ENSP00000299206.4:p.Gly442Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-198C>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.343G>C
  hgvsp: ENSP00000359187.3:p.Gly115Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1324G>C
  hgvsp: ENSP00000359181.3:p.Gly442Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1324G>C
  hgvsp: ENSP00000359188.1:p.Gly442Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.535G>C
  hgvsp: ENSP00000390810.2:p.Gly179Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1048G>C
  hgvsp: ENSP00000400676.1:p.Gly350Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.594G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1939G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.493G>C
  hgvsp: ENSP00000406791.1:p.Gly165Arg
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8799
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7721
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4947
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2714
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly442Arg
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

10-103340047-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340047
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340047
    reference: chr 10
allele count: 9
allele frequency: 7.437156031533541e-5
allele num: 121014
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1045C>T
  hgvsp: ENSP00000400676.1:p.Arg349Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.490C>T
  hgvsp: ENSP00000343102.3:p.Arg164Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.532C>T
  hgvsp: ENSP00000390810.2:p.Arg178Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.496C>T
  hgvsp: ENSP00000359177.3:p.Arg166Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1321C>T
  hgvsp: ENSP00000359188.1:p.Arg441Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.421G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.591C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1321C>T
  hgvsp: ENSP00000299206.4:p.Arg441Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1936C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1321C>T
  hgvsp: ENSP00000359181.3:p.Arg441Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1057C>T
  hgvsp: ENSP00000359191.1:p.Arg353Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.490C>T
  hgvsp: ENSP00000406791.1:p.Arg164Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.340C>T
  hgvsp: ENSP00000359187.3:p.Arg114Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.750C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-195G>A
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9610
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg441Trp
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

10-103340051-GGACCGGC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340051
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340044
    reference: chr 10
allele count: 4
allele frequency: 3.304255881575469e-5
allele num: 121056
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.739_745delGCCGGTC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.521_527delGCCGGTC
  hgvsp: ENSP00000390810.2:p.Gly174AlafsTer24
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.580_586delGCCGGTC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1310_1316delGCCGGTC
  hgvsp: ENSP00000359181.3:p.Gly437AlafsTer24
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1046_1052delGCCGGTC
  hgvsp: ENSP00000359191.1:p.Gly349AlafsTer24
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.426_432delGACCGGC
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1034_1040delGCCGGTC
  hgvsp: ENSP00000400676.1:p.Gly345AlafsTer31
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1925_1931delGCCGGTC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.479_485delGCCGGTC
  hgvsp: ENSP00000343102.3:p.Gly160AlafsTer24
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.485_491delGCCGGTC
  hgvsp: ENSP00000359177.3:p.Gly162AlafsTer24
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.329_335delGCCGGTC
  hgvsp: ENSP00000359187.3:p.Gly110AlafsTer24
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1310_1316delGCCGGTC
  hgvsp: ENSP00000299206.4:p.Gly437AlafsTer24
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.479_485delGCCGGTC
  hgvsp: ENSP00000406791.1:p.Gly160AlafsTer24
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1310_1316delGCCGGTC
  hgvsp: ENSP00000359188.1:p.Gly437AlafsTer24
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-190_-184delGACCGGC
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 3677
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1965
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9629
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10240
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
hgvs: p.Gly437AlafsTer24
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: GGACCGGC
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

10-103340056-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340056
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340056
    reference: chr 10
allele count: 20331
allele frequency: 1.678195265295341e-1
allele num: 121148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.481C>T
  hgvsp: ENSP00000343102.3:p.Arg161Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.741C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-186G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.331C>T
  hgvsp: ENSP00000359187.3:p.Arg111Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1036C>T
  hgvsp: ENSP00000400676.1:p.Arg346Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1927C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1312C>T
  hgvsp: ENSP00000299206.4:p.Arg438Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1048C>T
  hgvsp: ENSP00000359191.1:p.Arg350Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1312C>T
  hgvsp: ENSP00000359181.3:p.Arg438Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.582C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.523C>T
  hgvsp: ENSP00000390810.2:p.Arg175Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.487C>T
  hgvsp: ENSP00000359177.3:p.Arg163Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.430G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.481C>T
  hgvsp: ENSP00000406791.1:p.Arg161Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1312C>T
  hgvsp: ENSP00000359188.1:p.Arg438Trp
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8860
  bin: 2.75e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 6144
  bin: 3.75e1
  variant carriers: 281
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 4508
  bin: 4.25e1
  variant carriers: 286
genotype depth: GenotypeDepth
  all individuals: 1080
  bin: 7.25e1
  variant carriers: 726
genotype depth: GenotypeDepth
  all individuals: 10459
  bin: 9.75e1
  variant carriers: 10312
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 6.25e1
  variant carriers: 557
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 5.75e1
  variant carriers: 514
genotype depth: GenotypeDepth
  all individuals: 1049
  bin: 8.75e1
  variant carriers: 937
genotype quality: GenotypeQuality
hgvs: p.Arg438Trp
num of homozygotes: 2070
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ

10-103340059-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340059
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340059
    reference: chr 10
allele count: 4
allele frequency: 3.300711303285858e-5
allele num: 121186
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.478G>A
  hgvsp: ENSP00000343102.3:p.Gly160Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1033G>A
  hgvsp: ENSP00000400676.1:p.Gly345Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.433C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.738G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.579G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1309G>A
  hgvsp: ENSP00000359188.1:p.Gly437Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1309G>A
  hgvsp: ENSP00000359181.3:p.Gly437Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.328G>A
  hgvsp: ENSP00000359187.3:p.Gly110Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1045G>A
  hgvsp: ENSP00000359191.1:p.Gly349Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.520G>A
  hgvsp: ENSP00000390810.2:p.Gly174Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1309G>A
  hgvsp: ENSP00000299206.4:p.Gly437Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1924G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.478G>A
  hgvsp: ENSP00000406791.1:p.Gly160Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.484G>A
  hgvsp: ENSP00000359177.3:p.Gly162Ser
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-183C>T
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 4602
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1347
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6205
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly437Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

http://identifiers.org/exac.variant/10-103340062-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340062
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340062
    reference: chr 10
allele count: 1
allele frequency: 8.250552787036732e-6
allele num: 121204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.735G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.475G>T
  hgvsp: ENSP00000343102.3:p.Asp159Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.475G>T
  hgvsp: ENSP00000406791.1:p.Asp159Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.517G>T
  hgvsp: ENSP00000390810.2:p.Asp173Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.576G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1306G>T
  hgvsp: ENSP00000299206.4:p.Asp436Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1042G>T
  hgvsp: ENSP00000359191.1:p.Asp348Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-180C>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1306G>T
  hgvsp: ENSP00000359181.3:p.Asp436Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.325G>T
  hgvsp: ENSP00000359187.3:p.Asp109Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.481G>T
  hgvsp: ENSP00000359177.3:p.Asp161Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1921G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1030G>T
  hgvsp: ENSP00000400676.1:p.Asp344Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.436C>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1306G>T
  hgvsp: ENSP00000359188.1:p.Asp436Tyr
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6204
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9067
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1137
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6738
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp436Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

10-103340068-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340068
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340068
    reference: chr 10
allele count: 2
allele frequency: 1.649865535958819e-5
allele num: 121222
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1915C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.475C>T
  hgvsp: ENSP00000359177.3:p.His159Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+3G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.469C>T
  hgvsp: ENSP00000343102.3:p.His157Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1300C>T
  hgvsp: ENSP00000359181.3:p.His434Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+3G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.729C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1300C>T
  hgvsp: ENSP00000299206.4:p.His434Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.570C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.319C>T
  hgvsp: ENSP00000359187.3:p.His107Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.511C>T
  hgvsp: ENSP00000390810.2:p.His171Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1024C>T
  hgvsp: ENSP00000400676.1:p.His342Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1300C>T
  hgvsp: ENSP00000359188.1:p.His434Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1036C>T
  hgvsp: ENSP00000359191.1:p.His346Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.469C>T
  hgvsp: ENSP00000406791.1:p.His157Tyr
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 8986
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6202
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1157
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9067
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1884
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6762
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2534
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1348
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.His434Tyr
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum

10-103340070-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340070
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340070
    reference: chr 10
allele count: 2
allele frequency: 1.649729444371123e-5
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+5G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1022C>T
  hgvsp: ENSP00000400676.1:p.Thr341Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.473C>T
  hgvsp: ENSP00000359177.3:p.Thr158Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+5G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1034C>T
  hgvsp: ENSP00000359191.1:p.Thr345Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.467C>T
  hgvsp: ENSP00000343102.3:p.Thr156Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1298C>T
  hgvsp: ENSP00000299206.4:p.Thr433Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.317C>T
  hgvsp: ENSP00000359187.3:p.Thr106Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.467C>T
  hgvsp: ENSP00000406791.1:p.Thr156Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1298C>T
  hgvsp: ENSP00000359181.3:p.Thr433Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1298C>T
  hgvsp: ENSP00000359188.1:p.Thr433Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.509C>T
  hgvsp: ENSP00000390810.2:p.Thr170Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.568C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1913C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.727C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1885
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1243
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9067
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8118
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6774
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr433Ile
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-103340081-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340081
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340081
    reference: chr 10
allele count: 407
allele frequency: 3.356590298052023e-3
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1011C>T
  hgvsp: ENST00000415897.1:c.1011C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+16G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.557C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.462C>T
  hgvsp: ENST00000370158.3:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1023C>T
  hgvsp: ENST00000370172.1:c.1023C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.306C>T
  hgvsp: ENST00000370168.3:c.306C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.456C>T
  hgvsp: ENST00000429502.1:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1287C>T
  hgvsp: ENST00000299206.4:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.456C>T
  hgvsp: ENST00000339310.3:c.456C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1287C>T
  hgvsp: ENST00000370162.3:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1287C>T
  hgvsp: ENST00000370169.1:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+16G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.716C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1902C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.498C>T
  hgvsp: ENST00000456836.2:c.498C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4571
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 8.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 6752
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8983
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2499
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 7.75e1
  variant carriers: 17
genotype quality: GenotypeQuality
hgvs: p.Asp429Asp
num of homozygotes: 1
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ

10-103340083-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340083
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340083
    reference: chr 10
allele count: 1
allele frequency: 8.24715060946443e-6
allele num: 121254
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+18C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.496G>A
  hgvsp: ENSP00000390810.2:p.Asp166Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.454G>A
  hgvsp: ENSP00000343102.3:p.Asp152Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.454G>A
  hgvsp: ENSP00000406791.1:p.Asp152Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1021G>A
  hgvsp: ENSP00000359191.1:p.Asp341Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.1009G>A
  hgvsp: ENSP00000400676.1:p.Asp337Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1285G>A
  hgvsp: ENSP00000359188.1:p.Asp429Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1285G>A
  hgvsp: ENSP00000359181.3:p.Asp429Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.304G>A
  hgvsp: ENSP00000359187.3:p.Asp102Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.555G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1900G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.460G>A
  hgvsp: ENSP00000359177.3:p.Asp154Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1285G>A
  hgvsp: ENSP00000299206.4:p.Asp429Asn
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+18C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.714G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp429Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

10-103340093-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340093
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340093
    reference: chr 10
allele count: 1
allele frequency: 8.246742536698004e-6
allele num: 121260
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1275T>C
  hgvsp: ENST00000370162.3:c.1275T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.444T>C
  hgvsp: ENST00000429502.1:c.444T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.545T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.704T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+28A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1890T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+28A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.294T>C
  hgvsp: ENST00000370168.3:c.294T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1275T>C
  hgvsp: ENST00000299206.4:c.1275T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.486T>C
  hgvsp: ENST00000456836.2:c.486T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.999T>C
  hgvsp: ENST00000415897.1:c.999T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.444T>C
  hgvsp: ENST00000339310.3:c.444T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1275T>C
  hgvsp: ENST00000370169.1:c.1275T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.450T>C
  hgvsp: ENST00000370158.3:c.450T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1011T>C
  hgvsp: ENST00000370172.1:c.1011T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9066
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1550
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9062
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys425Cys
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum

10-103340094-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340094
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340094
    reference: chr 10
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.703G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.485G>A
  hgvsp: ENSP00000390810.2:p.Cys162Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.544G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1010G>A
  hgvsp: ENSP00000359191.1:p.Cys337Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1274G>A
  hgvsp: ENSP00000299206.4:p.Cys425Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.998G>A
  hgvsp: ENSP00000400676.1:p.Cys333Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1274G>A
  hgvsp: ENSP00000359188.1:p.Cys425Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1274G>A
  hgvsp: ENSP00000359181.3:p.Cys425Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.449G>A
  hgvsp: ENSP00000359177.3:p.Cys150Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.293G>A
  hgvsp: ENSP00000359187.3:p.Cys98Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+29C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+29C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.443G>A
  hgvsp: ENSP00000343102.3:p.Cys148Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.443G>A
  hgvsp: ENSP00000406791.1:p.Cys148Tyr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1889G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8150
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9061
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6216
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys425Tyr
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

10-103340096-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340096
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340096
    reference: chr 10
allele count: 1
allele frequency: 8.246606521416436e-6
allele num: 121262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.447C>A
  hgvsp: ENST00000370158.3:c.447C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+31G>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1008C>A
  hgvsp: ENST00000370172.1:c.1008C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.441C>A
  hgvsp: ENST00000339310.3:c.441C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1272C>A
  hgvsp: ENST00000299206.4:c.1272C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1272C>A
  hgvsp: ENST00000370162.3:c.1272C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.441C>A
  hgvsp: ENST00000429502.1:c.441C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1887C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.996C>A
  hgvsp: ENST00000415897.1:c.996C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+31G>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1272C>A
  hgvsp: ENST00000370169.1:c.1272C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.291C>A
  hgvsp: ENST00000370168.3:c.291C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.701C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.542C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.483C>A
  hgvsp: ENST00000456836.2:c.483C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr424Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

10-103340097-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340097
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340097
    reference: chr 10
allele count: 1
allele frequency: 8.246878556466378e-6
allele num: 121258
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.440C>T
  hgvsp: ENSP00000343102.3:p.Thr147Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+32G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1007C>T
  hgvsp: ENSP00000359191.1:p.Thr336Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1886C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1271C>T
  hgvsp: ENSP00000299206.4:p.Thr424Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.482C>T
  hgvsp: ENSP00000390810.2:p.Thr161Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.700C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.446C>T
  hgvsp: ENSP00000359177.3:p.Thr149Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1271C>T
  hgvsp: ENSP00000359181.3:p.Thr424Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.995C>T
  hgvsp: ENSP00000400676.1:p.Thr332Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.440C>T
  hgvsp: ENSP00000406791.1:p.Thr147Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1271C>T
  hgvsp: ENSP00000359188.1:p.Thr424Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.290C>T
  hgvsp: ENSP00000359187.3:p.Thr97Ile
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+32G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.541C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1135
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6216
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr424Ile
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-103340099-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340099
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340099
    reference: chr 10
allele count: 9
allele frequency: 7.4223131226496e-5
allele num: 121256
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1269G>A
  hgvsp: ENST00000370162.3:c.1269G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.438G>A
  hgvsp: ENST00000339310.3:c.438G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1269G>A
  hgvsp: ENST00000299206.4:c.1269G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+34C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.288G>A
  hgvsp: ENST00000370168.3:c.288G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.539G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.993G>A
  hgvsp: ENST00000415897.1:c.993G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1005G>A
  hgvsp: ENST00000370172.1:c.1005G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.480G>A
  hgvsp: ENST00000456836.2:c.480G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1269G>A
  hgvsp: ENST00000370169.1:c.1269G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+34C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.698G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.444G>A
  hgvsp: ENST00000370158.3:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1884G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.438G>A
  hgvsp: ENST00000429502.1:c.438G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6215
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6774
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9060
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9073
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2516
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala423Ala
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

10-103340100-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340100
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340100
    reference: chr 10
allele count: 5
allele frequency: 4.123575304732215e-5
allele num: 121254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.437C>T
  hgvsp: ENSP00000343102.3:p.Ala146Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1268C>T
  hgvsp: ENSP00000299206.4:p.Ala423Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.287C>T
  hgvsp: ENSP00000359187.3:p.Ala96Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1268C>T
  hgvsp: ENSP00000359181.3:p.Ala423Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.992C>T
  hgvsp: ENSP00000400676.1:p.Ala331Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+35G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1883C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.538C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.437C>T
  hgvsp: ENSP00000406791.1:p.Ala146Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.443C>T
  hgvsp: ENSP00000359177.3:p.Ala148Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1268C>T
  hgvsp: ENSP00000359188.1:p.Ala423Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1004C>T
  hgvsp: ENSP00000359191.1:p.Ala335Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.697C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+35G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.479C>T
  hgvsp: ENSP00000390810.2:p.Ala160Val
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1121
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4599
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8151
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala423Val
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum

10-103340102-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340102
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340102
    reference: chr 10
allele count: 2
allele frequency: 1.649402916144356e-5
allele num: 121256
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1266G>A
  hgvsp: ENST00000370162.3:c.1266G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.695G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+37C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+37C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.435G>A
  hgvsp: ENST00000429502.1:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.441G>A
  hgvsp: ENST00000370158.3:c.441G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.477G>A
  hgvsp: ENST00000456836.2:c.477G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.285G>A
  hgvsp: ENST00000370168.3:c.285G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.990G>A
  hgvsp: ENST00000415897.1:c.990G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1266G>A
  hgvsp: ENST00000299206.4:c.1266G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1266G>A
  hgvsp: ENST00000370169.1:c.1266G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.435G>A
  hgvsp: ENST00000339310.3:c.435G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.536G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1881G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.1002G>A
  hgvsp: ENST00000370172.1:c.1002G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6768
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9068
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys422Lys
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

10-103340109-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340109
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340109
    reference: chr 10
allele count: 1
allele frequency: 8.248102936324645e-6
allele num: 121240
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1259G>A
  hgvsp: ENSP00000359181.3:p.Arg420Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.470G>A
  hgvsp: ENSP00000390810.2:p.Arg157Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.529G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1874G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.428G>A
  hgvsp: ENSP00000406791.1:p.Arg143Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.434G>A
  hgvsp: ENSP00000359177.3:p.Arg145Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1259G>A
  hgvsp: ENSP00000359188.1:p.Arg420Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1259G>A
  hgvsp: ENSP00000299206.4:p.Arg420Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+44C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+44C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.278G>A
  hgvsp: ENSP00000359187.3:p.Arg93Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.995G>A
  hgvsp: ENSP00000359191.1:p.Arg332Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.983G>A
  hgvsp: ENSP00000400676.1:p.Arg328Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.428G>A
  hgvsp: ENSP00000343102.3:p.Arg143Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.688G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8147
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1229
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9071
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4597
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg420Gln
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
population: African
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

10-103340110-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340110
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340110
    reference: chr 10
allele count: 2
allele frequency: 1.649729444371123e-5
allele num: 121232
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.427C>T
  hgvsp: ENSP00000343102.3:p.Arg143Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.433C>T
  hgvsp: ENSP00000359177.3:p.Arg145Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.982C>T
  hgvsp: ENSP00000400676.1:p.Arg328Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.994C>T
  hgvsp: ENSP00000359191.1:p.Arg332Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1258C>T
  hgvsp: ENSP00000359181.3:p.Arg420Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1258C>T
  hgvsp: ENSP00000359188.1:p.Arg420Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1873C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.528C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.427C>T
  hgvsp: ENSP00000406791.1:p.Arg143Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1258C>T
  hgvsp: ENSP00000299206.4:p.Arg420Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+45G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.469C>T
  hgvsp: ENSP00000390810.2:p.Arg157Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.277C>T
  hgvsp: ENSP00000359187.3:p.Arg93Trp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.687C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+45G>A
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9067
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1865
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2517
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8146
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6755
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1549
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg420Trp
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

10-103340112-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340112
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340112
    reference: chr 10
allele count: 8
allele frequency: 6.59870005608895e-5
allele num: 121236
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.467G>A
  hgvsp: ENSP00000390810.2:p.Arg156Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1871G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.992G>A
  hgvsp: ENSP00000359191.1:p.Arg331Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.275G>A
  hgvsp: ENSP00000359187.3:p.Arg92Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.425G>A
  hgvsp: ENSP00000343102.3:p.Arg142Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1256G>A
  hgvsp: ENSP00000359188.1:p.Arg419Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.431G>A
  hgvsp: ENSP00000359177.3:p.Arg144Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1256G>A
  hgvsp: ENSP00000299206.4:p.Arg419Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.685G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.425G>A
  hgvsp: ENSP00000406791.1:p.Arg142Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1256G>A
  hgvsp: ENSP00000359181.3:p.Arg419Gln
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+47C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+47C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.526G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.980G>A
  hgvsp: ENSP00000400676.1:p.Arg327Gln
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1864
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6218
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9070
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6748
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg419Gln
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: Latino
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD

10-103340113-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340113
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340113
    reference: chr 10
allele count: 10
allele frequency: 8.248239000973292e-5
allele num: 121238
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1255C>T
  hgvsp: ENSP00000359188.1:p.Arg419Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.274C>T
  hgvsp: ENSP00000359187.3:p.Arg92Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.466C>T
  hgvsp: ENSP00000390810.2:p.Arg156Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.424C>T
  hgvsp: ENSP00000343102.3:p.Arg142Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.979C>T
  hgvsp: ENSP00000400676.1:p.Arg327Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.424C>T
  hgvsp: ENSP00000406791.1:p.Arg142Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1255C>T
  hgvsp: ENSP00000359181.3:p.Arg419Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.684C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+48G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.430C>T
  hgvsp: ENSP00000359177.3:p.Arg144Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.525C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1255C>T
  hgvsp: ENSP00000299206.4:p.Arg419Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.991C>T
  hgvsp: ENSP00000359191.1:p.Arg331Ter
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1870C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+48G>A
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1153
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1122
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8149
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4595
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg419Ter
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

10-103340117-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340117
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340117
    reference: chr 10
allele count: 65
allele frequency: 5.361620694206151e-4
allele num: 121232
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1866A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1251A>C
  hgvsp: ENST00000370169.1:c.1251A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.420A>C
  hgvsp: ENST00000339310.3:c.420A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.987A>C
  hgvsp: ENST00000370172.1:c.987A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.975A>C
  hgvsp: ENST00000415897.1:c.975A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.680A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1251A>C
  hgvsp: ENST00000370162.3:c.1251A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+52T>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.521A>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.462A>C
  hgvsp: ENST00000456836.2:c.462A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1251A>C
  hgvsp: ENST00000299206.4:c.1251A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+52T>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.420A>C
  hgvsp: ENST00000429502.1:c.420A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.426A>C
  hgvsp: ENST00000370158.3:c.426A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.270A>C
  hgvsp: ENST00000370168.3:c.270A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1136
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3486
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1548
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9049
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser417Ser
num of homozygotes: 0
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: DP

10-103340125-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340125
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340125
    reference: chr 10
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+60A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.454T>C
  hgvsp: ENSP00000390810.2:p.Cys152Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1243T>C
  hgvsp: ENSP00000359181.3:p.Cys415Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1858T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.412T>C
  hgvsp: ENSP00000343102.3:p.Cys138Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1243T>C
  hgvsp: ENSP00000359188.1:p.Cys415Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.418T>C
  hgvsp: ENSP00000359177.3:p.Cys140Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+60A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.979T>C
  hgvsp: ENSP00000359191.1:p.Cys327Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.412T>C
  hgvsp: ENSP00000406791.1:p.Cys138Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.262T>C
  hgvsp: ENSP00000359187.3:p.Cys88Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1243T>C
  hgvsp: ENSP00000299206.4:p.Cys415Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.967T>C
  hgvsp: ENSP00000400676.1:p.Cys323Arg
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.672T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.513T>C
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1151
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3487
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6222
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1862
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Cys415Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

10-103340128-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340128
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340128
    reference: chr 10
allele count: 56
allele frequency: 4.621072088724584e-4
allele num: 121184
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1240G>A
  hgvsp: ENSP00000299206.4:p.Ala414Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.976G>A
  hgvsp: ENSP00000359191.1:p.Ala326Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.409G>A
  hgvsp: ENSP00000343102.3:p.Ala137Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+63C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.415G>A
  hgvsp: ENSP00000359177.3:p.Ala139Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.451G>A
  hgvsp: ENSP00000390810.2:p.Ala151Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1240G>A
  hgvsp: ENSP00000359188.1:p.Ala414Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+63C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.259G>A
  hgvsp: ENSP00000359187.3:p.Ala87Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1855G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1240G>A
  hgvsp: ENSP00000359181.3:p.Ala414Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.409G>A
  hgvsp: ENSP00000406791.1:p.Ala137Thr
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.510G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.669G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.964G>A
  hgvsp: ENSP00000400676.1:p.Ala322Thr
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1233
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1239
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1867
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4591
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6213
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1325
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6610
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala414Thr
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum

10-103340135-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340135
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340135
    reference: chr 10
allele count: 1
allele frequency: 8.255320554097116e-6
allele num: 121134
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.408G>A
  hgvsp: ENST00000370158.3:c.408G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.444G>A
  hgvsp: ENST00000456836.2:c.444G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.402G>A
  hgvsp: ENST00000339310.3:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.969G>A
  hgvsp: ENST00000370172.1:c.969G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.503G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.957G>A
  hgvsp: ENST00000415897.1:c.957G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+70C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1233G>A
  hgvsp: ENST00000370162.3:c.1233G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.662G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+70C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1233G>A
  hgvsp: ENST00000370169.1:c.1233G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1848G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.252G>A
  hgvsp: ENST00000370168.3:c.252G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1233G>A
  hgvsp: ENST00000299206.4:c.1233G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.402G>A
  hgvsp: ENST00000429502.1:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1120
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2508
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3482
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1863
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6210
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4586
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu411Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

10-103340140-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340140
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340140
    reference: chr 10
allele count: 1
allele frequency: 8.258183860205463e-6
allele num: 121092
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.247C>G
  hgvsp: ENSP00000359187.3:p.Leu83Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1228C>G
  hgvsp: ENSP00000359188.1:p.Leu410Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.397C>G
  hgvsp: ENSP00000343102.3:p.Leu133Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.403C>G
  hgvsp: ENSP00000359177.3:p.Leu135Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1228C>G
  hgvsp: ENSP00000359181.3:p.Leu410Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1843C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1228C>G
  hgvsp: ENSP00000299206.4:p.Leu410Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.439C>G
  hgvsp: ENSP00000390810.2:p.Leu147Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.657C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.964C>G
  hgvsp: ENSP00000359191.1:p.Leu322Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.952C>G
  hgvsp: ENSP00000400676.1:p.Leu318Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.498C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+75G>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.397C>G
  hgvsp: ENSP00000406791.1:p.Leu133Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+75G>C
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8998
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8139
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9073
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1150
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu410Val
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ

10-103340141-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340141
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340141
    reference: chr 10
allele count: 3
allele frequency: 2.477373323644051e-5
allele num: 121096
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1227G>A
  hgvsp: ENST00000370162.3:c.1227G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.396G>A
  hgvsp: ENST00000429502.1:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.656G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.951G>A
  hgvsp: ENST00000415897.1:c.951G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1227G>A
  hgvsp: ENST00000370169.1:c.1227G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1842G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1227G>A
  hgvsp: ENST00000299206.4:c.1227G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.438G>A
  hgvsp: ENST00000456836.2:c.438G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+76C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.246G>A
  hgvsp: ENST00000370168.3:c.246G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.497G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.402G>A
  hgvsp: ENST00000370158.3:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+76C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.963G>A
  hgvsp: ENST00000370172.1:c.963G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.396G>A
  hgvsp: ENST00000339310.3:c.396G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3480
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1319
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2506
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6543
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1547
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6203
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly409Gly
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

10-103340144-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340144
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340144
    reference: chr 10
allele count: 27915
allele frequency: 2.306376720590908e-1
allele num: 121034
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.960T>C
  hgvsp: ENST00000370172.1:c.960T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.393T>C
  hgvsp: ENST00000339310.3:c.393T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+79A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+79A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1224T>C
  hgvsp: ENST00000370169.1:c.1224T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.435T>C
  hgvsp: ENST00000456836.2:c.435T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1839T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1224T>C
  hgvsp: ENST00000370162.3:c.1224T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.393T>C
  hgvsp: ENST00000429502.1:c.393T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1224T>C
  hgvsp: ENST00000299206.4:c.1224T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.494T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.243T>C
  hgvsp: ENST00000370168.3:c.243T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.948T>C
  hgvsp: ENST00000415897.1:c.948T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.399T>C
  hgvsp: ENST00000370158.3:c.399T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.653T>C
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1279
  bin: 6.25e1
  variant carriers: 813
genotype depth: GenotypeDepth
  all individuals: 7651
  bin: 3.25e1
  variant carriers: 291
genotype depth: GenotypeDepth
  all individuals: 12571
  bin: 9.75e1
  variant carriers: 12501
genotype depth: GenotypeDepth
  all individuals: 4063
  bin: 4.25e1
  variant carriers: 488
genotype depth: GenotypeDepth
  all individuals: 1286
  bin: 8.25e1
  variant carriers: 1236
genotype depth: GenotypeDepth
  all individuals: 5846
  bin: 2.25e1
  variant carriers: 200
genotype depth: GenotypeDepth
  all individuals: 1182
  bin: 6.75e1
  variant carriers: 909
genotype depth: GenotypeDepth
  all individuals: 5749
  bin: 3.75e1
  variant carriers: 410
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 5.75e1
  variant carriers: 765
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ser408Ser
num of homozygotes: 3633
population: African
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD

10-103340160-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340160
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340160
    reference: chr 10
allele count: 1
allele frequency: 8.295037908323241e-6
allele num: 120554
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.944C>T
  hgvsp: ENSP00000359191.1:p.Ala315Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.637C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+95G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.932C>T
  hgvsp: ENSP00000400676.1:p.Ala311Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.383C>T
  hgvsp: ENSP00000359177.3:p.Ala128Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.227C>T
  hgvsp: ENSP00000359187.3:p.Ala76Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.377C>T
  hgvsp: ENSP00000406791.1:p.Ala126Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1208C>T
  hgvsp: ENSP00000359188.1:p.Ala403Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1208C>T
  hgvsp: ENSP00000359181.3:p.Ala403Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.377C>T
  hgvsp: ENSP00000343102.3:p.Ala126Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.478C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+95G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1823C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1208C>T
  hgvsp: ENSP00000299206.4:p.Ala403Val
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.419C>T
  hgvsp: ENSP00000390810.2:p.Ala140Val
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8439
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2324
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5634
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala403Val
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff

10-103340172-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340172
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340172
    reference: chr 10
allele count: 1
allele frequency: 8.309512730173502e-6
allele num: 120344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.365T>A
  hgvsp: ENSP00000406791.1:p.Val122Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.365T>A
  hgvsp: ENSP00000343102.3:p.Val122Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.466T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.920T>A
  hgvsp: ENSP00000400676.1:p.Val307Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+107A>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.215T>A
  hgvsp: ENSP00000359187.3:p.Val72Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.371T>A
  hgvsp: ENSP00000359177.3:p.Val124Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1811T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1196T>A
  hgvsp: ENSP00000359181.3:p.Val399Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1196T>A
  hgvsp: ENSP00000359188.1:p.Val399Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1196T>A
  hgvsp: ENSP00000299206.4:p.Val399Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.407T>A
  hgvsp: ENSP00000390810.2:p.Val136Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.625T>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.932T>A
  hgvsp: ENSP00000359191.1:p.Val311Asp
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+107A>T
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4119
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2646
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1316
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 932
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val399Asp
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: DP

10-103340173-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340173
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340173
    reference: chr 10
allele count: 11
allele frequency: 9.145631713725099e-5
allele num: 120276
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.931G>C
  hgvsp: ENSP00000359191.1:p.Val311Leu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.214G>C
  hgvsp: ENSP00000359187.3:p.Val72Leu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.406G>C
  hgvsp: ENSP00000390810.2:p.Val136Leu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.370G>C
  hgvsp: ENSP00000359177.3:p.Val124Leu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1195G>C
  hgvsp: ENSP00000359181.3:p.Val399Leu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+108C>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.364G>C
  hgvsp: ENSP00000343102.3:p.Val122Leu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1195G>C
  hgvsp: ENSP00000299206.4:p.Val399Leu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.364G>C
  hgvsp: ENSP00000406791.1:p.Val122Leu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1195G>C
  hgvsp: ENSP00000359188.1:p.Val399Leu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.624G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.919G>C
  hgvsp: ENSP00000400676.1:p.Val307Leu
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.465G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+108C>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1810G>C
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 957
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4947
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8332
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val399Leu
num of homozygotes: 1
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ClippingRankSum

10-103340175-TGGGAAAGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340175
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340167
    reference: chr 10
allele count: 2
allele frequency: 1.663422991832593e-5
allele num: 120234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.364-10_364-3delTCTTTCCC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.406-10_406-3delTCTTTCCC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.364-10_364-3delTCTTTCCC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.624-10_624-3delTCTTTCCC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1195-10_1195-3delTCTTTCCC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.919-10_919-3delTCTTTCCC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1195-10_1195-3delTCTTTCCC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1195-10_1195-3delTCTTTCCC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.931-10_931-3delTCTTTCCC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.214-10_214-3delTCTTTCCC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.370-10_370-3delTCTTTCCC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.465-10_465-3delTCTTTCCC
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5484
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4945
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8294
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3394
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2986
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: c.1195-10_1195-3delTCTTTCCC
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
reference allele: TGGGAAAGA
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

10-103340179-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340179
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340179
    reference: chr 10
allele count: 27852
allele frequency: 2.320419895026243e-1
allele num: 120030
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.214-6T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.370-6T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1195-6T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.364-6T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.465-6T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1195-6T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.624-6T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.919-6T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.364-6T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+114A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1195-6T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+114A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.406-6T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1804T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.931-6T>C
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5148
  bin: 2.25e1
  variant carriers: 653
genotype depth: GenotypeDepth
  all individuals: 3481
  bin: 5.25e1
  variant carriers: 2077
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 5.75e1
  variant carriers: 2239
genotype depth: GenotypeDepth
  all individuals: 1352
  bin: 8.25e1
  variant carriers: 1303
genotype depth: GenotypeDepth
  all individuals: 2657
  bin: 6.25e1
  variant carriers: 2186
genotype depth: GenotypeDepth
  all individuals: 5032
  bin: 4.25e1
  variant carriers: 1470
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.5e0
  variant carriers: 45
genotype depth: GenotypeDepth
  all individuals: 8247
  bin: 3.25e1
  variant carriers: 950
genotype quality: GenotypeQuality
hgvs: c.1195-6T>C
num of homozygotes: 3614
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

10-103340184-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340184
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340184
    reference: chr 10
allele count: 3
allele frequency: 2.515470141369422e-5
allele num: 119262
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1195-11C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.624-11C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.465-11C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.406-11C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.214-11C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+119G>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1799C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.919-11C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1195-11C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.364-11C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+119G>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.931-11C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1195-11C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.364-11C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.370-11C>G
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6262
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14796
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8629
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2105
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12919
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP

10-103340185-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340185
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340185
    reference: chr 10
allele count: 1
allele frequency: 8.393063971933595e-6
allele num: 119146
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.370-12T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1195-12T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+120A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.624-12T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.919-12T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.364-12T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1195-12T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1798T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.465-12T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.406-12T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.214-12T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.931-12T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+120A>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.364-12T>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1195-12T>C
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2119
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5621
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2274
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-103340187-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340187
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340187
    reference: chr 10
allele count: 1
allele frequency: 8.408448809363649e-6
allele num: 118928
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.364-14G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.931-14G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.465-14G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+122C>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1195-14G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.214-14G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.370-14G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+122C>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.406-14G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1796G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.919-14G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.624-14G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1195-14G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.364-14G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1195-14G>T
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 688
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

10-103340187-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340187
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340187
    reference: chr 10
allele count: 1
allele frequency: 8.408448809363649e-6
allele num: 118928
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+122C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1195-14G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+122C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1195-14G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.919-14G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.406-14G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.364-14G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1195-14G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.364-14G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.214-14G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1796G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.465-14G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.931-14G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.370-14G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.624-14G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8617
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12861
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14606
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6070
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff

10-103340188-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340188
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340188
    reference: chr 10
allele count: 776
allele frequency: 6.528579360939577e-3
allele num: 118862
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.919-15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1195-15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+123G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.364-15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.406-15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.214-15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1795C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+123G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.364-15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1195-15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1195-15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.370-15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.465-15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.624-15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.931-15C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14415
  bin: 2.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 5909
  bin: 2.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1278
  bin: 5.75e1
  variant carriers: 108
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 6.25e1
  variant carriers: 64
genotype depth: GenotypeDepth
  all individuals: 8562
  bin: 3.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 2656
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3629
  bin: 4.75e1
  variant carriers: 95
genotype depth: GenotypeDepth
  all individuals: 5568
  bin: 4.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 7.25e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 1.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
num of homozygotes: 25
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

10-103340196-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340196
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340196
    reference: chr 10
allele count: 1
allele frequency: 8.446659346228567e-6
allele num: 118390
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+131G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.214-23C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.624-23C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.465-23C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1787C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+131G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1195-23C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.364-23C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.919-23C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.364-23C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.370-23C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1195-23C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.406-23C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1195-23C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.931-23C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5091
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1280
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1716
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8553
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13770
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2054
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum

10-103340209-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340209
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340209
    reference: chr 10
allele count: 5
allele frequency: 4.260177564200876e-5
allele num: 117366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.364-36G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1195-36G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.624-36G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.370-36G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1195-36G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.931-36G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.919-36G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.364-36G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1774G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+144C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1195-36G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+144C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.406-36G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.214-36G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.465-36G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3905
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11523
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8393
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1576
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2048
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4877
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

10-103340210-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340210
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340210
    reference: chr 10
allele count: 24
allele frequency: 2.043944813490036e-4
allele num: 117420
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.919-37C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+145G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.465-37C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.214-37C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1773C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.624-37C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1195-37C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.364-37C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.406-37C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.370-37C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.931-37C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.364-37C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1195-37C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1195-37C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+145G>A
  variant of: http://identifiers.org/hgnc/24542
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1621
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12020
  bin: 2.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
num of homozygotes: 1
population: European (Non-Finnish)
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: QD
site quality: MQ

10-103340210-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340210
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340210
    reference: chr 10
allele count: 1
allele frequency: 8.51643672287515e-6
allele num: 117420
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.406-37C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.465-37C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1773C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1195-37C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.364-37C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.214-37C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+145G>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.931-37C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.370-37C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+145G>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1195-37C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.364-37C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.919-37C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.624-37C>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1195-37C>A
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3548
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11324
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12020
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2049
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5520
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1177
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: South Asian
reference allele: G
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

10-103340220-C-CCT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340220
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340222
    reference: chr 10
allele count: 1
allele frequency: 8.574417368339821e-6
allele num: 116626
alternate allele: CCT
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1195-49_1195-48dupAG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+159_439+160dupTC
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1761_1762dupAG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.364-49_364-48dupAG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+159_-177+160dupTC
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.406-49_406-48dupAG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.214-49_214-48dupAG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.364-49_364-48dupAG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.370-49_370-48dupAG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.919-49_919-48dupAG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1195-49_1195-48dupAG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.624-49_624-48dupAG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.931-49_931-48dupAG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1195-49_1195-48dupAG
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.465-49_465-48dupAG
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5485
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10338
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5061
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

10-103340225-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103340225
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103340225
    reference: chr 10
allele count: 1
allele frequency: 8.614154779133072e-6
allele num: 116088
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000463515
  gene symbol: POLL
  hgvsc: ENST00000463515.1:n.1758G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+160C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1195-52G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.364-52G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.364-52G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.919-52G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.465-52G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.931-52G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.624-52G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.370-52G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.214-52G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.406-52G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+160C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1195-52G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1195-52G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5477
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7579
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10008
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2047
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8219
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1175
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
reference allele: C
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum

10-103342471-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103342471
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103342471
    reference: chr 10
allele count: 80
allele frequency: 6.599135513247764e-4
allele num: 121228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+2406C>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.918+49G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.405+49G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1194+49G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.464+49G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.623+49G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.213+49G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1194+49G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.363+49G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1194+49G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.369+49G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+2406C>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.930+49G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.363+49G>C
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.75e1
  variant carriers: 71
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32498
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

10-103342471-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103342471
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103342471
    reference: chr 10
allele count: 1
allele frequency: 8.248919391559706e-6
allele num: 121228
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.623+49G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.369+49G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.213+49G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1194+49G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.918+49G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.405+49G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1194+49G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1194+49G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.363+49G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.930+49G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+2406C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.363+49G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+2406C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.464+49G>A
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

10-103342478-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103342478
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103342478
    reference: chr 10
allele count: 2
allele frequency: 1.649103712132456e-5
allele num: 121278
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.363+42C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1194+42C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+2413G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.363+42C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.464+42C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.213+42C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1194+42C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.369+42C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+2413G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.405+42C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.918+42C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.623+42C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1194+42C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.930+42C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32631
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1619
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12246
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12449
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

10-103342488-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103342488
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103342488
    reference: chr 10
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.918+32C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.930+32C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.405+32C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.464+32C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.369+32C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.363+32C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1194+32C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1194+32C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+2423G>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+2423G>C
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.213+32C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.623+32C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1194+32C>G
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.363+32C>G
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12391
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1633
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12547
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/10-103342496-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103342496
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103342496
    reference: chr 10
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.464+24G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.363+24G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1194+24G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.405+24G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.363+24G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.213+24G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1194+24G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.369+24G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+2431C>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.918+24G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1194+24G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.930+24G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.623+24G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+2431C>A
  variant of: http://identifiers.org/hgnc/24542
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12588
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32958
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12379
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-103342503-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103342503
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103342503
    reference: chr 10
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+2438C>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1194+17G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.464+17G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.405+17G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+2438C>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.369+17G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.623+17G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1194+17G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1194+17G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.213+17G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.918+17G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.363+17G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.363+17G>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.930+17G>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ

10-103342503-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103342503
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103342503
    reference: chr 10
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.213+17G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1194+17G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1194+17G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1194+17G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.363+17G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.918+17G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+2438C>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.623+17G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+2438C>G
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.405+17G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.930+17G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.464+17G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.369+17G>C
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.363+17G>C
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

10-103342505-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103342505
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103342505
    reference: chr 10
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.623+15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.213+15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.369+15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+2440G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1194+15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.363+15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.405+15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.464+15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+2440G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.918+15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1194+15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1194+15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.930+15C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.363+15C>T
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33036
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

10-103342523-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103342523
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103342523
    reference: chr 10
allele count: 2
allele frequency: 1.647446457990115e-5
allele num: 121400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.915G>A
  hgvsp: ENST00000415897.1:c.915G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.461G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1191G>A
  hgvsp: ENST00000370162.3:c.1191G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1191G>A
  hgvsp: ENST00000370169.1:c.1191G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.210G>A
  hgvsp: ENST00000370168.3:c.210G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.927G>A
  hgvsp: ENST00000370172.1:c.927G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+2458C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.402G>A
  hgvsp: ENST00000456836.2:c.402G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1191G>A
  hgvsp: ENST00000299206.4:c.1191G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.360G>A
  hgvsp: ENST00000339310.3:c.360G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.366G>A
  hgvsp: ENST00000370158.3:c.366G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+2458C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.620G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.360G>A
  hgvsp: ENST00000429502.1:c.360G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12342
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln397Gln
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS

10-103342524-T-TAC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103342524
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103342526
    reference: chr 10
allele count: 1
allele frequency: 8.237096588194593e-6
allele num: 121402
alternate allele: TAC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.913_914insGT
  hgvsp: ENSP00000400676.1:p.Gln305ArgfsTer74
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.459_460insGT
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.208_209insGT
  hgvsp: ENSP00000359187.3:p.Gln70ArgfsTer67
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1189_1190insGT
  hgvsp: ENSP00000359188.1:p.Gln397ArgfsTer67
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1189_1190insGT
  hgvsp: ENSP00000299206.4:p.Gln397ArgfsTer67
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.364_365insGT
  hgvsp: ENSP00000359177.3:p.Gln122ArgfsTer67
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1189_1190insGT
  hgvsp: ENSP00000359181.3:p.Gln397ArgfsTer67
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.358_359insGT
  hgvsp: ENSP00000406791.1:p.Gln120ArgfsTer67
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.358_359insGT
  hgvsp: ENSP00000343102.3:p.Gln120ArgfsTer67
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.925_926insGT
  hgvsp: ENSP00000359191.1:p.Gln309ArgfsTer67
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.400_401insGT
  hgvsp: ENSP00000390810.2:p.Gln134ArgfsTer67
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+2459_-177+2460insAC
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+2459_439+2460insAC
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.618_619insGT
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1642
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33094
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln397ArgfsTer67
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: MQ

10-103342557-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103342557
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103342557
    reference: chr 10
allele count: 3
allele frequency: 2.471047559428694e-5
allele num: 121406
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.326G>A
  hgvsp: ENSP00000343102.3:p.Arg109His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.332G>A
  hgvsp: ENSP00000359177.3:p.Arg111His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000390810
  ensembl transcript: ENST00000456836
  gene symbol: POLL
  hgvsc: ENST00000456836.2:c.368G>A
  hgvsp: ENSP00000390810.2:p.Arg123His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.326G>A
  hgvsp: ENSP00000406791.1:p.Arg109His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.586G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.176G>A
  hgvsp: ENSP00000359187.3:p.Arg59His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1157G>A
  hgvsp: ENSP00000359188.1:p.Arg386His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.881G>A
  hgvsp: ENSP00000400676.1:p.Arg294His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+2492C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1157G>A
  hgvsp: ENSP00000359181.3:p.Arg386His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.893G>A
  hgvsp: ENSP00000359191.1:p.Arg298His
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+2492C>T
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.427G>A
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1157G>A
  hgvsp: ENSP00000299206.4:p.Arg386His
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12347
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg386His
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum

10-103342586-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 103342586
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 103342586
    reference: chr 10
allele count: 1
allele frequency: 8.238182327451271e-6
allele num: 121386
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359187
  ensembl transcript: ENST00000370168
  gene symbol: POLL
  hgvsc: ENST00000370168.3:c.147C>T
  hgvsp: ENST00000370168.3:c.147C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359181
  ensembl transcript: ENST00000370162
  gene symbol: POLL
  hgvsc: ENST00000370162.3:c.1128C>T
  hgvsp: ENST00000370162.3:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl protein: ENSP00000412584
  ensembl transcript: ENST00000416979
  gene symbol: DPCD
  hgvsc: ENST00000416979.2:c.-177+2521G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000485369
  gene symbol: POLL
  hgvsc: ENST00000485369.1:n.398C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000299206
  ensembl transcript: ENST00000299206
  gene symbol: POLL
  hgvsc: ENST00000299206.4:c.1128C>T
  hgvsp: ENST00000299206.4:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359191
  ensembl transcript: ENST00000370172
  gene symbol: POLL
  hgvsc: ENST00000370172.1:c.864C>T
  hgvsp: ENST00000370172.1:c.864C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359188
  ensembl transcript: ENST00000370169
  gene symbol: POLL
  hgvsc: ENST00000370169.1:c.1128C>T
  hgvsp: ENST00000370169.1:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000343102
  ensembl transcript: ENST00000339310
  gene symbol: POLL
  hgvsc: ENST00000339310.3:c.297C>T
  hgvsp: ENST00000339310.3:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000166169
  ensembl transcript: ENST00000470140
  gene symbol: POLL
  hgvsc: ENST00000470140.1:n.557C>T
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000400676
  ensembl transcript: ENST00000415897
  gene symbol: POLL
  hgvsc: ENST00000415897.1:c.852C>T
  hgvsp: ENST00000415897.1:c.852C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000166171
  ensembl transcript: ENST00000470165
  gene symbol: DPCD
  hgvsc: ENST00000470165.1:n.439+2521G>A
  variant of: http://identifiers.org/hgnc/24542
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000359177
  ensembl transcript: ENST00000370158
  gene symbol: POLL
  hgvsc: ENST00000370158.3:c.303C>T
  hgvsp: ENST00000370158.3:c.303C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000166169
  ensembl protein: ENSP00000406791
  ensembl transcript: ENST00000429502
  gene symbol: POLL
  hgvsc: ENST00000429502.1:c.297C>T
  hgvsp: ENST00000429502.1:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9184
canonical: true
consequence: synonymous
filter: PASS
hgvs: p.Gly376Gly
num of homozygotes: 0
reference allele: G

GenotypeDepth
all individuals: 8613
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 7712
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 348
bin: 1.25e1
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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bin: 9.75e1
variant carriers: 1

African
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allele count: 1
allele frequency: 9.663703131039814e-5
allele num: 10348
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: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66052
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 3.001e0

VQSLOD
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MQRankSum
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DP
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ReadPosRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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SIO_000300: 3.1e-3

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

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

Other
type: Population
allele count: 0
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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509753004408479e-5
allele num: 66236
num of homozygotes: 0

European (Finnish)
type: Population
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

ClippingRankSum
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SIO_000300: -2.59e-1

ReadPosRankSum
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SIO_000300: -2.79e-1

VQSLOD
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QD
type: SiteQuality
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FS
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SIO_000300: 4.554e0

MQ
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SIO_000300: 5.966e1

MQRankSum
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InbreedingCoeff
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SIO_000300: 3.8e-3

BaseQRankSum
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DP
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SIO_000300: 2.357445e6

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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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: 16200
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.509388395822013e-5
allele num: 66252
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10358
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: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.359144e6

MQRankSum
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SIO_000300: -4.73e-1

ClippingRankSum
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SIO_000300: -4.92e-1

QD
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SIO_000300: 1.681e1

BaseQRankSum
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SIO_000300: -2.412e0

InbreedingCoeff
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SIO_000300: 3.8e-3

MQ
type: SiteQuality
SIO_000300: 5.985e1

FS
type: SiteQuality
SIO_000300: 7.02e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.35e-1

ReadPosRankSum
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SIO_000300: 7.79e-1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

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

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

South Asian
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allele count: 2
allele frequency: 1.229256299938537e-4
allele num: 16270
num of homozygotes: 0

European (Non-Finnish)
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allele count: 4
allele frequency: 6.033364505716613e-5
allele num: 66298
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

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.25e-1

InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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ClippingRankSum
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FS
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QD
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MQ
type: SiteQuality
SIO_000300: 5.965e1

BaseQRankSum
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SIO_000300: 1.68e0

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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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: 6614
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Other
type: Population
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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: 2
allele frequency: 3.014045451805413e-5
allele num: 66356
num of homozygotes: 0

Latino
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num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

African
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allele count: 0
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allele num: 10368
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.03e-1

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506024096385542e-5
allele num: 66400
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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

Other
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Latino
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allele count: 0
allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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allele count: 0
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FS
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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ReadPosRankSum
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DP
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MQ
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QD
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MQRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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Other
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South Asian
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ReadPosRankSum
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MQ
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BaseQRankSum
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DP
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MQRankSum
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QD
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FS
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Latino
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East Asian
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African
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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QD
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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 (Finnish)
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Latino
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African
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South Asian
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European (Non-Finnish)
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MQRankSum
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MQ
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ReadPosRankSum
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InbreedingCoeff
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QD
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ClippingRankSum
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BaseQRankSum
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DP
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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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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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Latino
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African
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Other
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European (Finnish)
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European (Non-Finnish)
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East Asian
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FS
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VQSLOD
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InbreedingCoeff
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ClippingRankSum
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DP
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MQRankSum
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MQ
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BaseQRankSum
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QD
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ReadPosRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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East Asian
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European (Finnish)
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European (Non-Finnish)
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African
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South Asian
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Other
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FS
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InbreedingCoeff
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DP
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MQRankSum
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ReadPosRankSum
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MQ
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QD
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ClippingRankSum
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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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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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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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African
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East Asian
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QD
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InbreedingCoeff
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ClippingRankSum
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DP
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FS
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BaseQRankSum
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MQ
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MQRankSum
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VQSLOD
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ReadPosRankSum
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SIO_000300: 6.48e-1

GenotypeDepth
all individuals: 2405
bin: 5.25e1
variant carriers: 440

GenotypeDepth
all individuals: 6663
bin: 2.25e1
variant carriers: 101

GenotypeDepth
all individuals: 1286
bin: 6.75e1
variant carriers: 665

GenotypeDepth
all individuals: 107
bin: 7.5e0
variant carriers: 4

GenotypeDepth
all individuals: 8056
bin: 3.25e1
variant carriers: 199

GenotypeDepth
all individuals: 1111
bin: 7.75e1
variant carriers: 841

GenotypeDepth
all individuals: 3449
bin: 4.75e1
variant carriers: 390

GenotypeDepth
all individuals: 99
bin: 1.75e1
variant carriers: 52

GenotypeDepth
all individuals: 1057
bin: 8.25e1
variant carriers: 898

GenotypeDepth
all individuals: 986
bin: 9.25e1
variant carriers: 915

GenotypeQuality
all individuals: 37
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 4.75e1
variant carriers: 4

GenotypeQuality
all individuals: 129
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1511
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2845
bin: 8.25e1
variant carriers: 8

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2142
bin: 7.25e1
variant carriers: 7

GenotypeQuality
all individuals: 2364
bin: 9.25e1
variant carriers: 12

GenotypeQuality
all individuals: 36
bin: 3.25e1
variant carriers: 3

GenotypeQuality
all individuals: 4065
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 31880
bin: 9.75e1
variant carriers: 18203

GenotypeQuality
all individuals: 12455
bin: 6.25e1
variant carriers: 9

GenotypeQuality
all individuals: 18
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 33
bin: 5.25e1
variant carriers: 3

GenotypeQuality
all individuals: 3095
bin: 7.75e1
variant carriers: 3

East Asian
type: Population
allele count: 275
allele frequency: 3.182870370370371e-2
allele num: 8640
num of homozygotes: 7

South Asian
type: Population
allele count: 2017
allele frequency: 1.222868922032254e-1
allele num: 16494
num of homozygotes: 168

Latino
type: Population
allele count: 1132
allele frequency: 9.795777085496711e-2
allele num: 11556
num of homozygotes: 53

European (Finnish)
type: Population
allele count: 1266
allele frequency: 1.91412156032658e-1
allele num: 6614
num of homozygotes: 131

African
type: Population
allele count: 706
allele frequency: 6.804163454124904e-2
allele num: 10376
num of homozygotes: 20

European (Non-Finnish)
type: Population
allele count: 14777
allele frequency: 2.220035455665395e-1
allele num: 66562
num of homozygotes: 1682

Other
type: Population
allele count: 158
allele frequency: 1.7439293598234e-1
allele num: 906
num of homozygotes: 9

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

DP
type: SiteQuality
SIO_000300: 3.419992e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.09e-2

QD
type: SiteQuality
SIO_000300: 1.596e1

FS
type: SiteQuality
SIO_000300: 5.47e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.93e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

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

GenotypeDepth
all individuals: 2534
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1157
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variant carriers: 0

GenotypeDepth
all individuals: 1572
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variant carriers: 0

GenotypeDepth
all individuals: 8115
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variant carriers: 0

GenotypeDepth
all individuals: 1882
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variant carriers: 0

GenotypeDepth
all individuals: 1234
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variant carriers: 0

GenotypeDepth
all individuals: 3500
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 9069
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variant carriers: 3

GenotypeDepth
all individuals: 1243
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variant carriers: 0

GenotypeQuality
all individuals: 27
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 12766
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 3222
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variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2226
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variant carriers: 0

GenotypeQuality
all individuals: 30808
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 143
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 40
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 4223
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variant carriers: 0

GenotypeQuality
all individuals: 2519
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2982
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1610
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 5.25e1
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: 1
allele frequency: 1.502223290469895e-5
allele num: 66568
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 3
allele frequency: 2.592912705272256e-4
allele num: 11570
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10374
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.818e0

MQRankSum
type: SiteQuality
SIO_000300: -6.837e0

MQ
type: SiteQuality
SIO_000300: 5.089e1

FS
type: SiteQuality
SIO_000300: 7.832e0

DP
type: SiteQuality
SIO_000300: 3.286961e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.57e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.32e0

VQSLOD
type: SiteQuality
SIO_000300: -6.036e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.52e1

GenotypeDepth
all individuals: 8113
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2534
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 75
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variant carriers: 0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
all individuals: 3500
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variant carriers: 0

GenotypeDepth
all individuals: 1119
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variant carriers: 0

GenotypeDepth
all individuals: 1882
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variant carriers: 0

GenotypeDepth
all individuals: 1157
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variant carriers: 0

GenotypeDepth
all individuals: 8985
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variant carriers: 0

GenotypeDepth
all individuals: 4602
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 3222
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variant carriers: 0

GenotypeQuality
all individuals: 2982
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 36
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variant carriers: 0

GenotypeQuality
all individuals: 2231
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variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

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

GenotypeQuality
all individuals: 4221
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30805
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 26
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variant carriers: 0

GenotypeQuality
all individuals: 1609
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variant carriers: 0

GenotypeQuality
all individuals: 2519
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12802
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 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
allele num: 11570
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.15e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.25e-1

FS
type: SiteQuality
SIO_000300: 2.237e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -2.707e0

QD
type: SiteQuality
SIO_000300: 1.211e1

DP
type: SiteQuality
SIO_000300: 3.286901e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.56e-1

GenotypeDepth
all individuals: 1137
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 4604
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1233
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1569
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variant carriers: 1

GenotypeDepth
all individuals: 3500
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variant carriers: 0

GenotypeDepth
all individuals: 4
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variant carriers: 0

GenotypeDepth
all individuals: 90
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variant carriers: 0

GenotypeDepth
all individuals: 8117
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variant carriers: 0

GenotypeDepth
all individuals: 1243
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variant carriers: 0

GenotypeDepth
all individuals: 63
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variant carriers: 0

GenotypeDepth
all individuals: 1119
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variant carriers: 0

GenotypeQuality
all individuals: 30804
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variant carriers: 2

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 4214
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variant carriers: 0

GenotypeQuality
all individuals: 2229
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 1608
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 12845
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 2519
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 128
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variant carriers: 0

GenotypeQuality
all individuals: 2983
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 3224
bin: 7.75e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003453972067878e-5
allele num: 66590
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

FS
type: SiteQuality
SIO_000300: 5.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.298e0

QD
type: SiteQuality
SIO_000300: 2.753e1

DP
type: SiteQuality
SIO_000300: 3.287259e6

VQSLOD
type: SiteQuality
SIO_000300: -2.65e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.187e0

MQRankSum
type: SiteQuality
SIO_000300: 6.4e-2

GenotypeDepth
all individuals: 1347
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 8988
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1158
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 56
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variant carriers: 0

GenotypeDepth
all individuals: 1233
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1568
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variant carriers: 0

GenotypeDepth
all individuals: 2534
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variant carriers: 0

GenotypeDepth
all individuals: 4603
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variant carriers: 0

GenotypeDepth
all individuals: 1119
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1137
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 6201
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 122
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 31
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 1608
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variant carriers: 0

GenotypeQuality
all individuals: 2519
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2232
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variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 3226
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variant carriers: 0

GenotypeQuality
all individuals: 4216
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 12860
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30803
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2983
bin: 8.25e1
variant carriers: 0

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

African
type: Population
allele count: 2
allele frequency: 1.925669170036588e-4
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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.75e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

DP
type: SiteQuality
SIO_000300: 3.287325e6

MQRankSum
type: SiteQuality
SIO_000300: 1.61e0

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

QD
type: SiteQuality
SIO_000300: 1.193e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.111e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

GenotypeDepth
all individuals: 1551
bin: 6.25e1
variant carriers: 6

GenotypeDepth
all individuals: 1226
bin: 7.25e1
variant carriers: 9

GenotypeDepth
all individuals: 6171
bin: 3.75e1
variant carriers: 2

GenotypeDepth
all individuals: 1854
bin: 5.75e1
variant carriers: 8

GenotypeDepth
all individuals: 1158
bin: 8.25e1
variant carriers: 13

GenotypeDepth
all individuals: 3480
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variant carriers: 9

GenotypeDepth
all individuals: 8090
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variant carriers: 0

GenotypeDepth
all individuals: 9283
bin: 9.75e1
variant carriers: 271

GenotypeDepth
all individuals: 1132
bin: 9.25e1
variant carriers: 23

GenotypeDepth
all individuals: 1333
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variant carriers: 11

GenotypeQuality
all individuals: 29
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 2969
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variant carriers: 0

GenotypeQuality
all individuals: 3215
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variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 2.25e1
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GenotypeQuality
all individuals: 1601
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variant carriers: 0

GenotypeQuality
all individuals: 4204
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 1

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 14
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variant carriers: 0

GenotypeQuality
all individuals: 30889
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variant carriers: 406

GenotypeQuality
all individuals: 2507
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variant carriers: 0

GenotypeQuality
all individuals: 2214
bin: 7.25e1
variant carriers: 0

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

Other
type: Population
allele count: 4
allele frequency: 4.405286343612335e-3
allele num: 908
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 366
allele frequency: 5.494175573435811e-3
allele num: 66616
num of homozygotes: 1

Latino
type: Population
allele count: 14
allele frequency: 1.210025929127053e-3
allele num: 11570
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 4
allele frequency: 6.047777441790142e-4
allele num: 6614
num of homozygotes: 0

African
type: Population
allele count: 19
allele frequency: 1.82903350019253e-3
allele num: 10388
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.309426e6

VQSLOD
type: SiteQuality
SIO_000300: 4.66e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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SIO_000300: 1.64e0

FS
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SIO_000300: 5.3e-1

ReadPosRankSum
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MQ
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SIO_000300: 5.975e1

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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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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bin: 9.75e1
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.501185936890143e-5
allele num: 66614
num of homozygotes: 0

Latino
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num of homozygotes: 0

South Asian
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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

African
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Other
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num of homozygotes: 0

East Asian
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FS
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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QD
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MQRankSum
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MQ
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DP
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ReadPosRankSum
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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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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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South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (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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African
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.501095799933952e-5
allele num: 66618
num of homozygotes: 0

FS
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SIO_000300: 4.831e0

MQRankSum
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InbreedingCoeff
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DP
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VQSLOD
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ReadPosRankSum
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QD
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MQ
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SIO_000300: 6.0e1

ClippingRankSum
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SIO_000300: 3.91e-1

BaseQRankSum
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SIO_000300: 3.63e-1

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

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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MQ
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SIO_000300: 5.988e1

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

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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East Asian
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Other
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African
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South Asian
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European (Finnish)
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QD
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ReadPosRankSum
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DP
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ClippingRankSum
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FS
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MQ
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MQRankSum
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BaseQRankSum
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InbreedingCoeff
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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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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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Other
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European (Finnish)
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East Asian
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European (Non-Finnish)
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African
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South Asian
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VQSLOD
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QD
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MQRankSum
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MQ
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BaseQRankSum
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DP
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FS
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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African
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South Asian
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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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VQSLOD
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SIO_000300: 3.67e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

FS
type: SiteQuality
SIO_000300: 5.19e-1

DP
type: SiteQuality
SIO_000300: 3.285179e6

ClippingRankSum
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SIO_000300: -1.046e0

QD
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SIO_000300: 1.177e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 3.6e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.767e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.04e-1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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 count: 0
allele frequency: 0.0e0
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.501276084671971e-5
allele num: 66610
num of homozygotes: 0

Other
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allele num: 908
num of homozygotes: 0

South Asian
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allele count: 0
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num of homozygotes: 0

African
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allele frequency: 1.925298421255295e-4
allele num: 10388
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 6.28e-1

ClippingRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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DP
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BaseQRankSum
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SIO_000300: -4.47e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

FS
type: SiteQuality
SIO_000300: 1.731e0

QD
type: SiteQuality
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ReadPosRankSum
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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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8648
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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.002371873780286e-5
allele num: 66614
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.895e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.39e0

FS
type: SiteQuality
SIO_000300: 8.96e-1

DP
type: SiteQuality
SIO_000300: 3.284584e6

VQSLOD
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SIO_000300: 2.19e-1

QD
type: SiteQuality
SIO_000300: 1.326e1

MQRankSum
type: SiteQuality
SIO_000300: 3.56e-1

ClippingRankSum
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SIO_000300: 2.1e0

BaseQRankSum
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SIO_000300: -4.75e-1

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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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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
allele num: 66600
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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: 2

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
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allele num: 66592
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East Asian
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South Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

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

African
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allele frequency: 0.0e0
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Other
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BaseQRankSum
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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FS
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MQ
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InbreedingCoeff
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VQSLOD
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DP
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QD
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GenotypeDepth
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variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66594
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European (Finnish)
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Other
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South Asian
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Latino
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allele num: 11576
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QD
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MQRankSum
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ReadPosRankSum
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FS
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ClippingRankSum
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InbreedingCoeff
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MQ
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DP
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BaseQRankSum
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VQSLOD
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GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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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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allele frequency: 9.628345850182938e-5
allele num: 10386
num of homozygotes: 0

East Asian
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South Asian
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allele frequency: 1.817080557238038e-4
allele num: 16510
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Latino
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European (Non-Finnish)
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allele count: 6
allele frequency: 9.009550123130518e-5
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.284773e6

VQSLOD
type: SiteQuality
SIO_000300: 7.25e-1

FS
type: SiteQuality
SIO_000300: 5.26e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.44e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

QD
type: SiteQuality
SIO_000300: 1.135e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.89e-1

GenotypeDepth
all individuals: 1154
bin: 8.25e1
variant carriers: 3

GenotypeDepth
all individuals: 1229
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variant carriers: 3

GenotypeDepth
all individuals: 1122
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variant carriers: 3

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 9105
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variant carriers: 41

GenotypeDepth
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variant carriers: 2

GenotypeDepth
all individuals: 2510
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variant carriers: 0

GenotypeDepth
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variant carriers: 3

GenotypeQuality
all individuals: 4226
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variant carriers: 0

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 2220
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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GenotypeQuality
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variant carriers: 65

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 61
allele frequency: 5.873290968611593e-3
allele num: 10386
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.727712508638562e-4
allele num: 11576
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.003453972067878e-5
allele num: 66590
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.95e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.84e0

MQRankSum
type: SiteQuality
SIO_000300: 3.96e-1

QD
type: SiteQuality
SIO_000300: 1.263e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.09e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.43e-1

DP
type: SiteQuality
SIO_000300: 3.288325e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 93
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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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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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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2520
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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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variant carriers: 0

GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
all individuals: 1614
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501817198810561e-5
allele num: 66586
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: 904
num of homozygotes: 0

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -6.54e-1

QD
type: SiteQuality
SIO_000300: 1.092e1

MQRankSum
type: SiteQuality
SIO_000300: -5.76e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.25e-1

DP
type: SiteQuality
SIO_000300: 3.283412e6

FS
type: SiteQuality
SIO_000300: 3.224e0

MQ
type: SiteQuality
SIO_000300: 5.922e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.69e-1

GenotypeDepth
all individuals: 9091
bin: 9.75e1
variant carriers: 19

GenotypeDepth
all individuals: 105
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variant carriers: 0

GenotypeDepth
all individuals: 132
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variant carriers: 0

GenotypeDepth
all individuals: 1132
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variant carriers: 0

GenotypeDepth
all individuals: 3482
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variant carriers: 1

GenotypeDepth
all individuals: 1151
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variant carriers: 1

GenotypeDepth
all individuals: 1551
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variant carriers: 4

GenotypeDepth
all individuals: 1123
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variant carriers: 3

GenotypeDepth
all individuals: 8144
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variant carriers: 0

GenotypeDepth
all individuals: 9033
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variant carriers: 2

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1613
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variant carriers: 0

GenotypeQuality
all individuals: 2215
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 17
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GenotypeQuality
all individuals: 23
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 4217
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 12773
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2520
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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
all individuals: 28
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variant carriers: 0

GenotypeQuality
all individuals: 30677
bin: 9.75e1
variant carriers: 56

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
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: 56
allele frequency: 3.393528057205187e-3
allele num: 16502
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.971e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.08e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.63e-1

FS
type: SiteQuality
SIO_000300: 2.604e0

DP
type: SiteQuality
SIO_000300: 3.284757e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.559e0

QD
type: SiteQuality
SIO_000300: 1.067e1

MQRankSum
type: SiteQuality
SIO_000300: 4.11e-1

GenotypeDepth
all individuals: 125
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 9008
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variant carriers: 0

GenotypeDepth
all individuals: 8152
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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: 1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeQuality
all individuals: 24
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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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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
all individuals: 12618
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variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.647526807333103e-5
allele num: 11564
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66532
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.951e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.383e0

VQSLOD
type: SiteQuality
SIO_000300: -2.305e0

DP
type: SiteQuality
SIO_000300: 3.280595e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

MQRankSum
type: SiteQuality
SIO_000300: -2.04e-1

FS
type: SiteQuality
SIO_000300: 2.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.92e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.29e-1

QD
type: SiteQuality
SIO_000300: 2.809e1

GenotypeDepth
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bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1120
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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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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
all individuals: 1237
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variant carriers: 0

GenotypeDepth
all individuals: 1133
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variant carriers: 0

GenotypeQuality
all individuals: 107
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 9
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 898
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503759398496241e-5
allele num: 66500
num of homozygotes: 0

African
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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num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -3.11e-1

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 6.7e-1

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.982e0

VQSLOD
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SIO_000300: -2.721e0

InbreedingCoeff
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SIO_000300: 5.999999999999999e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.2e-2

DP
type: SiteQuality
SIO_000300: 3.279877e6

MQ
type: SiteQuality
SIO_000300: 5.877e1

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 140
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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
all individuals: 73
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 75
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GenotypeQuality
all individuals: 2999
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 3

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

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.729505361466621e-4
allele num: 11564
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503623733197005e-5
allele num: 66506
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 1.1e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

FS
type: SiteQuality
SIO_000300: 7.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.262e0

VQSLOD
type: SiteQuality
SIO_000300: -2.008e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.92e0

QD
type: SiteQuality
SIO_000300: 1.962e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.177e0

DP
type: SiteQuality
SIO_000300: 3.279745e6

GenotypeDepth
all individuals: 1379
bin: 8.75e1
variant carriers: 1348

GenotypeDepth
all individuals: 8483
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variant carriers: 250

GenotypeDepth
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variant carriers: 20

GenotypeDepth
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variant carriers: 109

GenotypeDepth
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variant carriers: 1180

GenotypeDepth
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variant carriers: 55

GenotypeDepth
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variant carriers: 1095

GenotypeDepth
all individuals: 2998
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variant carriers: 585

GenotypeDepth
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variant carriers: 646

GenotypeDepth
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variant carriers: 1412

GenotypeQuality
all individuals: 73
bin: 3.25e1
variant carriers: 6

GenotypeQuality
all individuals: 264
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variant carriers: 2

GenotypeQuality
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variant carriers: 12

GenotypeQuality
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variant carriers: 24

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 9

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 10

GenotypeQuality
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GenotypeQuality
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variant carriers: 18

GenotypeQuality
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variant carriers: 21

GenotypeQuality
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variant carriers: 8

GenotypeQuality
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variant carriers: 4

GenotypeQuality
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variant carriers: 21

GenotypeQuality
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variant carriers: 17

GenotypeQuality
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variant carriers: 24117

GenotypeQuality
all individuals: 1970
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variant carriers: 19

GenotypeQuality
all individuals: 27
bin: 5.25e1
variant carriers: 7

African
type: Population
allele count: 1892
allele frequency: 1.824493731918997e-1
allele num: 10370
num of homozygotes: 146

European (Finnish)
type: Population
allele count: 1657
allele frequency: 2.505291805261566e-1
allele num: 6614
num of homozygotes: 224

Latino
type: Population
allele count: 1678
allele frequency: 1.451808271327219e-1
allele num: 11558
num of homozygotes: 130

Other
type: Population
allele count: 209
allele frequency: 2.32739420935412e-1
allele num: 898
num of homozygotes: 19

South Asian
type: Population
allele count: 2740
allele frequency: 1.663025006069434e-1
allele num: 16476
num of homozygotes: 288

East Asian
type: Population
allele count: 287
allele frequency: 3.323297823066235e-2
allele num: 8636
num of homozygotes: 9

European (Non-Finnish)
type: Population
allele count: 19452
allele frequency: 2.925904756174604e-1
allele num: 66482
num of homozygotes: 2817

MQ
type: SiteQuality
SIO_000300: 5.964e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 9.6e-2

DP
type: SiteQuality
SIO_000300: 3.624064e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.88e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.76e0

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e-1

FS
type: SiteQuality
SIO_000300: 5.72e-1

QD
type: SiteQuality
SIO_000300: 1.593e1

GenotypeDepth
all individuals: 1879
bin: 7.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
all individuals: 12
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
all individuals: 4371
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variant carriers: 0

GenotypeQuality
all individuals: 28498
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66228
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10324
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 892
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.39e-1

DP
type: SiteQuality
SIO_000300: 2.746939e6

MQRankSum
type: SiteQuality
SIO_000300: -4.12e-1

FS
type: SiteQuality
SIO_000300: 7.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.82e-1

MQ
type: SiteQuality
SIO_000300: 5.95e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.82e-1

QD
type: SiteQuality
SIO_000300: 1.17e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.708e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.7e-3

GenotypeDepth
all individuals: 486
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variant carriers: 0

GenotypeDepth
all individuals: 2986
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variant carriers: 0

GenotypeDepth
all individuals: 1878
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variant carriers: 0

GenotypeDepth
all individuals: 9000
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variant carriers: 0

GenotypeDepth
all individuals: 6444
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 5569
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 2325
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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
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 6
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GenotypeQuality
all individuals: 270
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 233
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variant carriers: 0

GenotypeQuality
all individuals: 2894
bin: 9.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510984859931704e-5
allele num: 66182
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16136
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 886
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.58e0

VQSLOD
type: SiteQuality
SIO_000300: 1.34e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

FS
type: SiteQuality
SIO_000300: 3.079e0

QD
type: SiteQuality
SIO_000300: 1.465e1

MQRankSum
type: SiteQuality
SIO_000300: -1.29e-1

DP
type: SiteQuality
SIO_000300: 2.739992e6

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 2644
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variant carriers: 1

GenotypeDepth
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variant carriers: 1

GenotypeDepth
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variant carriers: 2

GenotypeDepth
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GenotypeDepth
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variant carriers: 2

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: 10

GenotypeQuality
all individuals: 324
bin: 3.75e1
variant carriers: 0

Other
type: Population
allele count: 2
allele frequency: 2.262443438914027e-3
allele num: 884
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66164
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.594927265945542e-4
allele num: 16086
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 1.62e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e-1

FS
type: SiteQuality
SIO_000300: 1.679e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.09e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.17e0

DP
type: SiteQuality
SIO_000300: 2.739588e6

QD
type: SiteQuality
SIO_000300: 1.65e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.4e-2

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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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: 2.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16070
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.023888720895071e-5
allele num: 66140
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10346
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -4.557e0

QD
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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DP
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ClippingRankSum
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BaseQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.307e1

VQSLOD
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SIO_000300: 1.55e0

GenotypeDepth
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variant carriers: 887

GenotypeDepth
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variant carriers: 176

GenotypeDepth
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variant carriers: 976

GenotypeDepth
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variant carriers: 2082

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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variant carriers: 53

GenotypeQuality
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GenotypeQuality
all individuals: 75
bin: 4.25e1
variant carriers: 16

GenotypeQuality
all individuals: 1957
bin: 7.25e1
variant carriers: 45

GenotypeQuality
all individuals: 2964
bin: 7.75e1
variant carriers: 83

GenotypeQuality
all individuals: 1111
bin: 2.25e1
variant carriers: 11

GenotypeQuality
all individuals: 282
bin: 2.75e1
variant carriers: 10

GenotypeQuality
all individuals: 2692
bin: 8.25e1
variant carriers: 82

European (Finnish)
type: Population
allele count: 1654
allele frequency: 2.503026634382566e-1
allele num: 6608
num of homozygotes: 222

African
type: Population
allele count: 1890
allele frequency: 1.829268292682927e-1
allele num: 10332
num of homozygotes: 145

East Asian
type: Population
allele count: 287
allele frequency: 3.328694038506147e-2
allele num: 8622
num of homozygotes: 9

European (Non-Finnish)
type: Population
allele count: 19403
allele frequency: 2.936022758224132e-1
allele num: 66086
num of homozygotes: 2803

Latino
type: Population
allele count: 1672
allele frequency: 1.449124631651933e-1
allele num: 11538
num of homozygotes: 128

Other
type: Population
allele count: 210
allele frequency: 2.380952380952381e-1
allele num: 882
num of homozygotes: 20

South Asian
type: Population
allele count: 2736
allele frequency: 1.714070918431274e-1
allele num: 15962
num of homozygotes: 287

DP
type: SiteQuality
SIO_000300: 2.730903e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.55e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.86e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.57e0

MQ
type: SiteQuality
SIO_000300: 5.97e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.3e-2

QD
type: SiteQuality
SIO_000300: 1.695e1

GenotypeDepth
all individuals: 2120
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3655
bin: 4.75e1
variant carriers: 1

GenotypeDepth
all individuals: 1229
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 5621
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 377
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 182
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variant carriers: 0

GenotypeDepth
all individuals: 82
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 92
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4944
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17817
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variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 661
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2082
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 533
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4303
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13863
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3388
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3262
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2117
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variant carriers: 0

GenotypeQuality
all individuals: 6860
bin: 6.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.732801940738174e-4
allele num: 11542
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.522023682688503e-5
allele num: 65702
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10290
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15618
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: -5.555e-1

MQ
type: SiteQuality
SIO_000300: 5.949e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 1.5091e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.05e-1

QD
type: SiteQuality
SIO_000300: 1.717e1

DP
type: SiteQuality
SIO_000300: 2.016015e6

GenotypeDepth
all individuals: 8618
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 1229
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 60
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 14672
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variant carriers: 0

GenotypeDepth
all individuals: 752
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variant carriers: 0

GenotypeDepth
all individuals: 46
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variant carriers: 0

GenotypeDepth
all individuals: 12884
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variant carriers: 0

GenotypeDepth
all individuals: 156
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variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
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variant carriers: 0

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

GenotypeQuality
all individuals: 583
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17458
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
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variant carriers: 0

GenotypeQuality
all individuals: 2191
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6843
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3388
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2116
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3259
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13862
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 116
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4942
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 738
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4303
bin: 8.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523275651961979e-5
allele num: 65648
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15566
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 874
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
allele num: 11538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10288
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 4.616e0

QD
type: SiteQuality
SIO_000300: 9.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.419e0

DP
type: SiteQuality
SIO_000300: 2.011924e6

MQRankSum
type: SiteQuality
SIO_000300: -1.027e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 8.46e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.84e-1

GenotypeDepth
all individuals: 1227
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2378
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12861
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 14606
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variant carriers: 0

GenotypeDepth
all individuals: 376
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variant carriers: 0

GenotypeDepth
all individuals: 5628
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 70
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variant carriers: 0

GenotypeDepth
all individuals: 156
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variant carriers: 0

GenotypeQuality
all individuals: 146
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variant carriers: 0

GenotypeQuality
all individuals: 2114
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variant carriers: 0

GenotypeQuality
all individuals: 4292
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17336
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4911
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6786
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3236
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variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3381
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13854
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 129
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2251
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 1.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65578
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.725734292939116e-5
allele num: 10282
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15448
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.381e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.04e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.75e0

DP
type: SiteQuality
SIO_000300: 2.009831e6

MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-2

GenotypeDepth
all individuals: 5628
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2120
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 688
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 24
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variant carriers: 0

GenotypeDepth
all individuals: 46
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variant carriers: 0

GenotypeDepth
all individuals: 376
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 783
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variant carriers: 0

GenotypeDepth
all individuals: 1227
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
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variant carriers: 0

GenotypeQuality
all individuals: 6786
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4911
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 378
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 129
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variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 93
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variant carriers: 0

GenotypeQuality
all individuals: 68
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variant carriers: 0

GenotypeQuality
all individuals: 3236
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variant carriers: 0

GenotypeQuality
all individuals: 4292
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2251
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2114
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variant carriers: 0

GenotypeQuality
all individuals: 774
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17336
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13854
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3381
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65578
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.47332988089073e-5
allele num: 15448
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 5.75e0

MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.6e-1

DP
type: SiteQuality
SIO_000300: 2.009831e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.04e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.4e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.381e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

GenotypeDepth
all individuals: 1141
bin: 7.5e0
variant carriers: 1

GenotypeDepth
all individuals: 35
bin: 9.25e1
variant carriers: 14

GenotypeDepth
all individuals: 2117
bin: 5.25e1
variant carriers: 90

GenotypeDepth
all individuals: 386
bin: 6.75e1
variant carriers: 49

GenotypeDepth
all individuals: 173
bin: 7.75e1
variant carriers: 42

GenotypeDepth
all individuals: 54
bin: 8.75e1
variant carriers: 20

GenotypeDepth
all individuals: 12713
bin: 3.25e1
variant carriers: 27

GenotypeDepth
all individuals: 105
bin: 9.75e1
variant carriers: 33

GenotypeQuality
all individuals: 68
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 198
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 451
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 41
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4890
bin: 7.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2089
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 701
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2437
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3337
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3189
bin: 7.25e1
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GenotypeQuality
all individuals: 16909
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 3.25e1
variant carriers: 1

GenotypeQuality
all individuals: 6719
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4249
bin: 8.25e1
variant carriers: 2

GenotypeQuality
all individuals: 14027
bin: 9.75e1
variant carriers: 742

European (Finnish)
type: Population
allele count: 127
allele frequency: 1.920750151240169e-2
allele num: 6612
num of homozygotes: 2

Other
type: Population
allele count: 7
allele frequency: 8.027522935779817e-3
allele num: 872
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 53
allele frequency: 8.084690951247789e-4
allele num: 65556
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.601456815816858e-4
allele num: 11532
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
num of homozygotes: 0

South Asian
type: Population
allele count: 32
allele frequency: 2.074688796680498e-3
allele num: 15424
num of homozygotes: 1

East Asian
type: Population
allele count: 554
allele frequency: 6.446357924133116e-2
allele num: 8594
num of homozygotes: 22

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.03e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.73e0

FS
type: SiteQuality
SIO_000300: 1.981e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.59e-2

QD
type: SiteQuality
SIO_000300: 1.496e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e-1

DP
type: SiteQuality
SIO_000300: 2.009983e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.3e-2

GenotypeDepth
all individuals: 643
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3743
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12565
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 132
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variant carriers: 1

GenotypeDepth
all individuals: 74
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GenotypeDepth
all individuals: 34
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GenotypeDepth
all individuals: 5566
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variant carriers: 0

GenotypeDepth
all individuals: 3566
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variant carriers: 0

GenotypeQuality
all individuals: 4281
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variant carriers: 0

GenotypeQuality
all individuals: 354
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GenotypeQuality
all individuals: 78
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GenotypeQuality
all individuals: 3158
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3376
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15352
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1015
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 823
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4892
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2907
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6451
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13428
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2105
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1423
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 257
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.583278472679394e-5
allele num: 15190
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 870
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European (Finnish)
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European (Non-Finnish)
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African
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Latino
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allele frequency: 0.0e0
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FS
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VQSLOD
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BaseQRankSum
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InbreedingCoeff
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QD
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DP
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ClippingRankSum
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MQ
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ReadPosRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 65028
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African
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Other
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Latino
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South Asian
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European (Finnish)
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East Asian
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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DP
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MQ
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FS
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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QD
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 65034
num of homozygotes: 0

South Asian
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Other
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Latino
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allele frequency: 1.740038280842178e-3
allele num: 11494
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European (Finnish)
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African
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East Asian
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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DP
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FS
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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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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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allele num: 65034
num of homozygotes: 0

European (Finnish)
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African
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Latino
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Other
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East Asian
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South Asian
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ReadPosRankSum
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VQSLOD
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QD
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DP
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MQRankSum
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FS
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BaseQRankSum
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InbreedingCoeff
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MQ
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ClippingRankSum
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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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African
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Latino
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European (Finnish)
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East Asian
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South Asian
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European (Non-Finnish)
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ClippingRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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MQ
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VQSLOD
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FS
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MQRankSum
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BaseQRankSum
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QD
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GenotypeDepth
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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 (Non-Finnish)
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Other
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South Asian
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Latino
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European (Finnish)
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African
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East Asian
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QD
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DP
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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FS
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MQ
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MQRankSum
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ReadPosRankSum
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Latino
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Other
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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FS
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MQRankSum
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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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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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SIO_000300: 8.4e-1

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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variant carriers: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
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: 66652
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Latino
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allele num: 11576
num of homozygotes: 0

African
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South Asian
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East Asian
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FS
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BaseQRankSum
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DP
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InbreedingCoeff
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MQRankSum
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VQSLOD
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ClippingRankSum
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ReadPosRankSum
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8652
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

African
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Other
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Latino
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South Asian
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European (Non-Finnish)
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allele num: 66678
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QD
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ReadPosRankSum
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MQ
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VQSLOD
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DP
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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FS
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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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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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South Asian
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East Asian
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Latino
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African
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European (Finnish)
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European (Non-Finnish)
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BaseQRankSum
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VQSLOD
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MQ
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FS
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MQRankSum
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DP
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ReadPosRankSum
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QD
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InbreedingCoeff
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Other
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East Asian
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European (Non-Finnish)
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European (Finnish)
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DP
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ClippingRankSum
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MQRankSum
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VQSLOD
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FS
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BaseQRankSum
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QD
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InbreedingCoeff
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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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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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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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Latino
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African
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Other
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QD
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InbreedingCoeff
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MQRankSum
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FS
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MQ
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ReadPosRankSum
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DP
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeDepth
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
all individuals: 11
bin: 3.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.155802126675913e-4
allele num: 8652
num of homozygotes: 0

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

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

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: 2.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.53e-1

QD
type: SiteQuality
SIO_000300: 1.842e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.642e0

DP
type: SiteQuality
SIO_000300: 1.688749e6

FS
type: SiteQuality
SIO_000300: 5.802e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.2e0

GenotypeDepth
all individuals: 72
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 9.75e1
variant carriers: 2

GenotypeDepth
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 12
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1642
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variant carriers: 0

GenotypeDepth
all individuals: 39
bin: 6.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 321
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.609840476648087e-5
allele num: 10406
num of homozygotes: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.882e0

DP
type: SiteQuality
SIO_000300: 1.689594e6

QD
type: SiteQuality
SIO_000300: 1.197e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.12e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.21e0

MQ
type: SiteQuality
SIO_000300: 5.983e1

VQSLOD
type: SiteQuality
SIO_000300: -5.001e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 3.18e0

GenotypeDepth
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bin: 4.25e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 22
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variant carriers: 0

GenotypeDepth
all individuals: 20
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variant carriers: 0

GenotypeDepth
all individuals: 111
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variant carriers: 1

GenotypeDepth
all individuals: 72
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GenotypeDepth
all individuals: 14
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GenotypeDepth
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GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 284
bin: 8.75e1
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GenotypeQuality
all individuals: 969
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GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 321
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variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

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

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

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

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

Latino
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allele count: 1
allele frequency: 8.637070305752289e-5
allele num: 11578
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66732
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.088e0

InbreedingCoeff
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SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.983e0

MQRankSum
type: SiteQuality
SIO_000300: 1.42e0

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.16e-1

QD
type: SiteQuality
SIO_000300: 1.458e1

DP
type: SiteQuality
SIO_000300: 1.688901e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.641e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

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

GenotypeDepth
all individuals: 75
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 22
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variant carriers: 0

GenotypeDepth
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
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variant carriers: 0

GenotypeDepth
all individuals: 110
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variant carriers: 3

GenotypeQuality
all individuals: 2111
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 321
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 2234
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variant carriers: 0

GenotypeQuality
all individuals: 4
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GenotypeQuality
all individuals: 44881
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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: 7
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 284
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.495055439017081e-5
allele num: 66740
num of homozygotes: 0

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

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

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

QD
type: SiteQuality
SIO_000300: 1.427e1

FS
type: SiteQuality
SIO_000300: 4.229e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.36e-1

ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 1.688882e6

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 1.83e0

ClippingRankSum
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SIO_000300: -1.154e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.84e-1