18-51818356-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818356
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818356
    reference: chr 18
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*447A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1043A>G
  hgvsp: ENSP00000462681.1:p.Tyr348Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.404A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.531A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1115A>G
  hgvsp: ENSP00000385196.3:p.Tyr372Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.974A>G
  hgvsp: ENSP00000217800.5:p.Tyr325Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4575A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.621A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1352A>G
  hgvsp: ENSP00000462664.1:p.Tyr451Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*333A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6148
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 315
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 385
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 432
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Tyr451Cys
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: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: QD

18-51818366-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818366
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818366
    reference: chr 18
allele count: 1
allele frequency: 8.261185645363822e-6
allele num: 121048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.414G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.631G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1125G>A
  hgvsp: ENSP00000385196.3:p.Met375Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*343G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1053G>A
  hgvsp: ENSP00000462681.1:p.Met351Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4585G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.984G>A
  hgvsp: ENSP00000217800.5:p.Met328Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.541G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*457G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1362G>A
  hgvsp: ENSP00000462664.1:p.Met454Ile
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48199
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Met454Ile
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

18-51818366-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818366
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818366
    reference: chr 18
allele count: 1
allele frequency: 8.261185645363822e-6
allele num: 121048
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1125G>C
  hgvsp: ENSP00000385196.3:p.Met375Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.541G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1053G>C
  hgvsp: ENSP00000462681.1:p.Met351Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.984G>C
  hgvsp: ENSP00000217800.5:p.Met328Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.631G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*343G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*457G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4585G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.414G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1362G>C
  hgvsp: ENSP00000462664.1:p.Met454Ile
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2550
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Met454Ile
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

18-51818369-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818369
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818369
    reference: chr 18
allele count: 31
allele frequency: 2.561390752553128e-4
allele num: 121028
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.544A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*346A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.417A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1128A>G
  hgvsp: ENST00000406285.3:c.1128A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4588A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1365A>G
  hgvsp: ENST00000579534.1:c.1365A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1056A>G
  hgvsp: ENST00000579434.1:c.1056A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.634A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.987A>G
  hgvsp: ENST00000217800.5:c.987A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*460A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48911
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 628
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6138
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 9.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 152
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 2544
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 855
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Pro455Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP

18-51818379-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818379
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818379
    reference: chr 18
allele count: 35
allele frequency: 2.894954507857734e-4
allele num: 120900
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*356A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.554A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4598A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.997A>G
  hgvsp: ENSP00000217800.5:p.Thr333Ala
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1138A>G
  hgvsp: ENSP00000385196.3:p.Thr380Ala
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.427A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1375A>G
  hgvsp: ENSP00000462664.1:p.Thr459Ala
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1066A>G
  hgvsp: ENSP00000462681.1:p.Thr356Ala
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*470A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.644A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6102
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 630
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 9.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 389
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2551
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48735
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr459Ala
num of homozygotes: 0
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum

18-51818380-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818380
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818380
    reference: chr 18
allele count: 1
allele frequency: 8.27417299640901e-6
allele num: 120858
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.998C>T
  hgvsp: ENSP00000217800.5:p.Thr333Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1376C>T
  hgvsp: ENSP00000462664.1:p.Thr459Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*357C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.555C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4599C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1139C>T
  hgvsp: ENSP00000385196.3:p.Thr380Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1067C>T
  hgvsp: ENSP00000462681.1:p.Thr356Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.428C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.645C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*471C>T
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2558
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48673
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6092
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr459Ile
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum

18-51818383-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818383
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818383
    reference: chr 18
allele count: 1
allele frequency: 8.277049397430804e-6
allele num: 120816
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.648C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1001C>T
  hgvsp: ENSP00000217800.5:p.Thr334Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1142C>T
  hgvsp: ENSP00000385196.3:p.Thr381Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.431C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1070C>T
  hgvsp: ENSP00000462681.1:p.Thr357Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*360C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1379C>T
  hgvsp: ENSP00000462664.1:p.Thr460Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.558C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*474C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4602C>T
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6098
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48601
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 307
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr460Ile
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

18-51818388-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818388
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818388
    reference: chr 18
allele count: 1
allele frequency: 8.285416010737898e-6
allele num: 120694
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4607C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*365C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.653C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*479C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1006C>T
  hgvsp: ENSP00000217800.5:p.Arg336Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.436C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1147C>T
  hgvsp: ENSP00000385196.3:p.Arg383Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1075C>T
  hgvsp: ENSP00000462681.1:p.Arg359Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1384C>T
  hgvsp: ENSP00000462664.1:p.Arg462Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.563C>T
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 393
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48475
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg462Cys
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD

18-51818389-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818389
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818389
    reference: chr 18
allele count: 15
allele frequency: 1.243904866155837e-4
allele num: 120588
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4608G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.564G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.654G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*366G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1076G>A
  hgvsp: ENSP00000462681.1:p.Arg359His
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1007G>A
  hgvsp: ENSP00000217800.5:p.Arg336His
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1385G>A
  hgvsp: ENSP00000462664.1:p.Arg462His
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1148G>A
  hgvsp: ENSP00000385196.3:p.Arg383His
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*480G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.437G>A
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2559
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 420
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 639
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48366
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 206
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 9.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 659
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 384
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg462His
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum

http://identifiers.org/exac.variant/18-51818390-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818390
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818390
    reference: chr 18
allele count: 2
allele frequency: 1.658237293756736e-5
allele num: 120610
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1008C>A
  hgvsp: ENST00000217800.5:c.1008C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*481C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1149C>A
  hgvsp: ENST00000406285.3:c.1149C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1386C>A
  hgvsp: ENST00000579534.1:c.1386C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1077C>A
  hgvsp: ENST00000579434.1:c.1077C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*367C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.565C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.438C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4609C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.655C>A
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 419
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6069
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 207
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2577
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg462Arg
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

18-51818391-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818391
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818391
    reference: chr 18
allele count: 16
allele frequency: 1.326787846623325e-4
allele num: 120592
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1078T>C
  hgvsp: ENSP00000462681.1:p.Ser360Pro
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1387T>C
  hgvsp: ENSP00000462664.1:p.Ser463Pro
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.439T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*368T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4610T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1150T>C
  hgvsp: ENSP00000385196.3:p.Ser384Pro
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.566T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1009T>C
  hgvsp: ENSP00000217800.5:p.Ser337Pro
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.656T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*482T>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48327
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 634
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 5401
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ser463Pro
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: Latino
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP

18-51818392-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818392
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818392
    reference: chr 18
allele count: 1
allele frequency: 8.295037908323241e-6
allele num: 120554
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.440C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.657C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*369C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1010C>G
  hgvsp: ENSP00000217800.5:p.Ser337Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.567C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1151C>G
  hgvsp: ENSP00000385196.3:p.Ser384Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*483C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1388C>G
  hgvsp: ENSP00000462664.1:p.Ser463Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1079C>G
  hgvsp: ENSP00000462681.1:p.Ser360Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4611C>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2573
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48252
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6058
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 638
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser463Cys
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum

18-51818401-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818401
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818401
    reference: chr 18
allele count: 2
allele frequency: 1.666194578202842e-5
allele num: 120034
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1397A>T
  hgvsp: ENSP00000462664.1:p.His466Leu
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1160A>T
  hgvsp: ENSP00000385196.3:p.His387Leu
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*492A>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.576A>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1019A>T
  hgvsp: ENSP00000217800.5:p.His340Leu
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4620A>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1088A>T
  hgvsp: ENSP00000462681.1:p.His363Leu
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*378A>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.666A>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.449A>T
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2530
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47585
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5931
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 641
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5328
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His466Leu
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

18-51818407-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818407
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818407
    reference: chr 18
allele count: 1
allele frequency: 8.353660574063554e-6
allele num: 119708
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1166T>G
  hgvsp: ENSP00000385196.3:p.Phe389Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1403T>G
  hgvsp: ENSP00000462664.1:p.Phe468Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*384T>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.672T>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1025T>G
  hgvsp: ENSP00000217800.5:p.Phe342Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*498T>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4626T>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.582T>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1094T>G
  hgvsp: ENSP00000462681.1:p.Phe365Cys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.455T>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 650
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5847
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1042
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Phe468Cys
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

18-51818416-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818416
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818416
    reference: chr 18
allele count: 3
allele frequency: 2.545911266505991e-5
allele num: 117836
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.673+8C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*385+8C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1026+8C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4635C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.583+8C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1095+8C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1167+8C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.456+8C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*499+8C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1404+8C>T
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2535
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45144
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 187
  bin: 4.25e1
  variant carriers: 0
hgvs: c.1404+8C>T
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS

18-51818417-ACT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818417
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818415
    reference: chr 18
allele count: 6775
allele frequency: 5.69279892446013e-2
allele num: 119010
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*499+12_*499+13delCT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.583+12_583+13delCT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4639_333+4640delCT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.456+12_456+13delCT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1026+12_1026+13delCT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.673+12_673+13delCT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1095+12_1095+13delCT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1167+12_1167+13delCT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*385+12_*385+13delCT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1404+12_1404+13delCT
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1832
  bin: 1.25e1
  variant carriers: 122
genotype depth: GenotypeDepth
  all individuals: 41329
  bin: 2.25e1
  variant carriers: 175
genotype depth: GenotypeDepth
  all individuals: 861
  bin: 3.75e1
  variant carriers: 307
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 2.75e1
  variant carriers: 168
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 9.25e1
  variant carriers: 190
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 7.75e1
  variant carriers: 298
genotype depth: GenotypeDepth
  all individuals: 540
  bin: 6.75e1
  variant carriers: 405
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 5.75e1
  variant carriers: 558
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.75e1
  variant carriers: 507
genotype depth: GenotypeDepth
  all individuals: 619
  bin: 1.75e1
  variant carriers: 183
genotype depth: GenotypeDepth
  all individuals: 442
  bin: 7.25e1
  variant carriers: 354
genotype depth: GenotypeDepth
  all individuals: 293
  bin: 8.25e1
  variant carriers: 240
genotype depth: GenotypeDepth
  all individuals: 1342
  bin: 9.75e1
  variant carriers: 1064
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 7.5e0
  variant carriers: 33
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 6.25e1
  variant carriers: 525
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 8.75e1
  variant carriers: 200
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 4.25e1
  variant carriers: 419
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 5.25e1
  variant carriers: 621
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 3.25e1
  variant carriers: 223
genotype quality: GenotypeQuality
  all individuals: 761
  bin: 8.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 1230
  bin: 7.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 40053
  bin: 6.25e1
  variant carriers: 6
num of homozygotes: 225
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: ACT
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ

18-51818420-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818420
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818421
    reference: chr 18
allele count: 126
allele frequency: 1.192301141202521e-3
allele num: 105678
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.673+18dupT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*499+18dupT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1095+18dupT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4645dupT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1026+18dupT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1167+18dupT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1404+18dupT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.456+18dupT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.583+18dupT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*385+18dupT
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5196
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2363
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 40799
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2086
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 7.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 9.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 6.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 7.5e0
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 676
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 416
  bin: 7.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 714
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 532
  bin: 6.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 8.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1318
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 3.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4569
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 502
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 2
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum

18-51818423-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818423
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818423
    reference: chr 18
allele count: 3
allele frequency: 2.535797000997414e-5
allele num: 118306
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.583+15T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1404+15T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*385+15T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1026+15T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4642T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.456+15T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*499+15T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1095+15T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.673+15T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1167+15T>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40007
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5088
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 633
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1050
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 453
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1891
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41381
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/18-51818430-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818430
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818430
    reference: chr 18
allele count: 1
allele frequency: 8.47314014573801e-6
allele num: 118020
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1026+22C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1095+22C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1167+22C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4649C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*385+22C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*499+22C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.583+22C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.456+22C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.673+22C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1404+22C>A
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1253
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2848
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 921
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4971
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3189
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 291
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD

18-51818436-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818436
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818436
    reference: chr 18
allele count: 1
allele frequency: 8.516291665956975e-6
allele num: 117422
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*385+28T>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1026+28T>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*499+28T>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1095+28T>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.583+28T>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.456+28T>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1167+28T>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4655T>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1404+28T>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.673+28T>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 620
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1322
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1397
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4975
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1773
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 544
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3288
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: T
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-51818439-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818439
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818439
    reference: chr 18
allele count: 2
allele frequency: 1.713913550200528e-5
allele num: 116692
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1167+31A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.583+31A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1095+31A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1026+31A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.673+31A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*499+31A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4658A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.456+31A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*385+31A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1404+31A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3594
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2065
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 382
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1096
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: A
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD

18-51818445-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818445
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818445
    reference: chr 18
allele count: 1
allele frequency: 8.619352169490942e-6
allele num: 116018
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1095+37A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.673+37A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*385+37A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4664A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*499+37A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1026+37A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1404+37A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1167+37A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.456+37A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.583+37A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3556
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1337
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2875
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 599
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/18-51818446-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818446
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818446
    reference: chr 18
allele count: 1
allele frequency: 8.642444774777888e-6
allele num: 115708
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1026+38C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1404+38C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1095+38C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4665C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.456+38C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1167+38C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.673+38C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*385+38C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.583+38C>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*499+38C>A
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3328
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1327
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 733
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 249
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ

18-51818448-CTT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818448
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818446
    reference: chr 18
allele count: 6317
allele frequency: 5.443061970083408e-2
allele num: 116056
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*499+41_*499+42delTT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.673+41_673+42delTT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1026+41_1026+42delTT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1167+41_1167+42delTT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4668_333+4669delTT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.456+41_456+42delTT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*385+41_*385+42delTT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.583+41_583+42delTT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1095+41_1095+42delTT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1404+41_1404+42delTT
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 9.75e1
  variant carriers: 195
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.75e1
  variant carriers: 73
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 6.75e1
  variant carriers: 117
genotype depth: GenotypeDepth
  all individuals: 5250
  bin: 2.75e1
  variant carriers: 922
genotype depth: GenotypeDepth
  all individuals: 490
  bin: 5.25e1
  variant carriers: 290
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.25e1
  variant carriers: 98
genotype depth: GenotypeDepth
  all individuals: 1774
  bin: 7.5e0
  variant carriers: 104
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 1.25e1
  variant carriers: 233
genotype depth: GenotypeDepth
  all individuals: 2985
  bin: 3.25e1
  variant carriers: 934
genotype depth: GenotypeDepth
  all individuals: 343
  bin: 6.25e1
  variant carriers: 170
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 3.75e1
  variant carriers: 760
genotype depth: GenotypeDepth
  all individuals: 3541
  bin: 1.75e1
  variant carriers: 385
genotype depth: GenotypeDepth
  all individuals: 37508
  bin: 2.25e1
  variant carriers: 676
genotype depth: GenotypeDepth
  all individuals: 904
  bin: 4.25e1
  variant carriers: 523
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 2.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.25e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 8.75e1
  variant carriers: 50
genotype depth: GenotypeDepth
  all individuals: 397
  bin: 5.75e1
  variant carriers: 224
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.25e1
  variant carriers: 56
genotype depth: GenotypeDepth
  all individuals: 680
  bin: 4.75e1
  variant carriers: 395
genotype quality: GenotypeQuality
  all individuals: 34470
  bin: 6.25e1
  variant carriers: 18
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.75e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 1545
  bin: 3.25e1
  variant carriers: 8
num of homozygotes: 177
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: CTT
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum

18-51818450-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818450
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818450
    reference: chr 18
allele count: 109
allele frequency: 1.046627746197573e-3
allele num: 104144
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1404+42T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.673+42T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*385+42T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.456+42T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1095+42T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1167+42T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*499+42T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4669T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1026+42T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.583+42T>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4339
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 4.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 36804
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1756
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 1.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2075
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 5.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 615
  bin: 3.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3147
  bin: 1.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1228
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 395
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33712
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 1
population: European (Finnish)
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: FS
site quality: QD

18-51818452-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818452
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818452
    reference: chr 18
allele count: 1
allele frequency: 8.708222303498963e-6
allele num: 114834
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*385+44T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1026+44T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.673+44T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1167+44T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.583+44T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4671T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*499+44T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1095+44T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.456+44T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1404+44T>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2010
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5510
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 597
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 763
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3500
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1181
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2984
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 636
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3587
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff

18-51818456-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51818456
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51818456
    reference: chr 18
allele count: 6
allele frequency: 5.197235070942259e-5
allele num: 115446
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.456+48A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1095+48A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.673+48A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1404+48A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+4675A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*385+48A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1167+48A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*499+48A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1026+48A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.583+48A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6123
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2956
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3493
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 508
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36921
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 531
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3698
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 1841
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP

18-51819969-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51819969
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51819969
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 27374
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.674-50A>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1168-50A>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*386-50A>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1405-50A>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.584-50A>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1027-50A>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6188A>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1096-50A>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.457-50A>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*500-50A>T
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29542
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9256
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 679
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16498
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 254
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-51819981-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51819981
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51819981
    reference: chr 18
allele count: 3
allele frequency: 1.061571125265393e-4
allele num: 28260
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*386-38T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1405-38T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*500-38T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1168-38T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1096-38T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.674-38T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.457-38T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1027-38T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6200T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.584-38T>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14718
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31022
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9488
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 726
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 124
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/18-51819983-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51819983
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51819983
    reference: chr 18
allele count: 1
allele frequency: 3.496259002866932e-5
allele num: 28602
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.584-36A>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1405-36A>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1027-36A>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.674-36A>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*500-36A>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*386-36A>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1096-36A>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1168-36A>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.457-36A>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6202A>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 489
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9571
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31670
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13862
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1627
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1148
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4265
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: DP

18-51819984-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51819984
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51819984
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 28784
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1405-35G>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*386-35G>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.674-35G>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1096-35G>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1168-35G>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.457-35G>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*500-35G>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6203G>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1027-35G>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.584-35G>T
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9606
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31911
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13512
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1924
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10930
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

18-51819988-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51819988
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51819988
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 29712
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1405-31T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.584-31T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.674-31T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6207T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1096-31T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1027-31T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*500-31T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.457-31T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*386-31T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1168-31T>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1037
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9583
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33150
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11944
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3827
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 424
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 99
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum

18-51819989-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51819989
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51819989
    reference: chr 18
allele count: 14139
allele frequency: 3.42332090455668e-1
allele num: 41302
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.457-30G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1168-30G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1405-30G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.674-30G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.584-30G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1027-30G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6208G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*500-30G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1096-30G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*386-30G>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 377
  bin: 3.25e1
  variant carriers: 162
genotype depth: GenotypeDepth
  all individuals: 3418
  bin: 1.75e1
  variant carriers: 2717
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 2.75e1
  variant carriers: 334
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 13374
  bin: 1.25e1
  variant carriers: 7586
genotype depth: GenotypeDepth
  all individuals: 8517
  bin: 2.5e0
  variant carriers: 651
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 4.25e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 2204
  bin: 2.25e1
  variant carriers: 833
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 7.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 8.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 76
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 3.75e1
  variant carriers: 144
genotype depth: GenotypeDepth
  all individuals: 29458
  bin: 7.5e0
  variant carriers: 8045
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 49
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 8.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 6.25e1
  variant carriers: 62
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 66
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 7.75e1
  variant carriers: 31
genotype quality: GenotypeQuality
  all individuals: 6231
  bin: 7.5e0
  variant carriers: 263
genotype quality: GenotypeQuality
  all individuals: 602
  bin: 8.75e1
  variant carriers: 548
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 3.75e1
  variant carriers: 443
num of homozygotes: 1861
population: Latino
population: East Asian
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

18-51819993-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51819993
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51819993
    reference: chr 18
allele count: 1
allele frequency: 2.31932461267279e-5
allele num: 43116
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*500-26A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1027-26A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1168-26A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.584-26A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1405-26A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.674-26A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.457-26A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1096-26A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6212A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*386-26A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 384
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13114
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2819
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8329
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30224
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1386
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4533
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: African
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

18-51819998-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51819998
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51819998
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 44044
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1096-21T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1027-21T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*500-21T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6217T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1168-21T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.674-21T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.457-21T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.584-21T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*386-21T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1405-21T>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: intron
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 12882
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30961
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2653
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 794
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 407
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4017
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 931
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2755
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum

18-51820022-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820022
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820022
    reference: chr 18
allele count: 1
allele frequency: 1.727712508638563e-5
allele num: 57880
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1099A>G
  hgvsp: ENSP00000462681.1:p.Met367Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.677A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1030A>G
  hgvsp: ENSP00000217800.5:p.Met344Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1408A>G
  hgvsp: ENSP00000462664.1:p.Met470Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6241A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*503A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*389A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1171A>G
  hgvsp: ENSP00000385196.3:p.Met391Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.587A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.460A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1478
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1530
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15068
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29103
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2330
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9015
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29278
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Met470Val
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: QD

18-51820030-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820030
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820030
    reference: chr 18
allele count: 37
allele frequency: 5.8059251820236e-4
allele num: 63728
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1038C>G
  hgvsp: ENSP00000217800.5:p.Asp346Glu
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.468C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.595C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1416C>G
  hgvsp: ENSP00000462664.1:p.Asp472Glu
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6249C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.685C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1179C>G
  hgvsp: ENSP00000385196.3:p.Asp393Glu
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1107C>G
  hgvsp: ENSP00000462681.1:p.Asp369Glu
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*397C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*511C>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1822
  bin: 1.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 553
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18397
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26685
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1690
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7974
  bin: 1.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1908
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1312
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 312
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Asp472Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

18-51820032-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820032
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820032
    reference: chr 18
allele count: 1
allele frequency: 1.532895947023116e-5
allele num: 65236
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1109C>G
  hgvsp: ENSP00000462681.1:p.Thr370Ser
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.470C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1418C>G
  hgvsp: ENSP00000462664.1:p.Thr473Ser
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*399C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1181C>G
  hgvsp: ENSP00000385196.3:p.Thr394Ser
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*513C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6251C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1040C>G
  hgvsp: ENSP00000217800.5:p.Thr347Ser
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.687C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.597C>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 557
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26083
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19087
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7790
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17953
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 310
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr473Ser
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: Other
reference allele: C
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

18-51820035-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820035
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820035
    reference: chr 18
allele count: 42
allele frequency: 6.194324818594773e-4
allele num: 67804
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1112A>G
  hgvsp: ENSP00000462681.1:p.His371Arg
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.690A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*402A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6254A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1421A>G
  hgvsp: ENSP00000462664.1:p.His474Arg
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.600A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1043A>G
  hgvsp: ENSP00000217800.5:p.His348Arg
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1184A>G
  hgvsp: ENSP00000385196.3:p.His395Arg
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*516A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.473A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1415
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25041
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2223
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7578
  bin: 1.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20093
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2115
  bin: 1.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 583
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1286
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 485
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His474Arg
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-51820049-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820049
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820049
    reference: chr 18
allele count: 1
allele frequency: 1.310203867721818e-5
allele num: 76324
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1057C>G
  hgvsp: ENSP00000217800.5:p.Pro353Ala
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.704C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.614C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1198C>G
  hgvsp: ENSP00000385196.3:p.Pro400Ala
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1435C>G
  hgvsp: ENSP00000462664.1:p.Pro479Ala
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.487C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*530C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*416C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6268C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1126C>G
  hgvsp: ENSP00000462681.1:p.Pro376Ala
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24281
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6585
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2936
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 963
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1220
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 377
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro479Ala
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD

18-51820051-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820051
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820051
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 77736
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1059C>T
  hgvsp: ENST00000217800.5:c.1059C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.489C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1128C>T
  hgvsp: ENST00000579434.1:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.616C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1437C>T
  hgvsp: ENST00000579534.1:c.1437C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*532C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.706C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*418C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1200C>T
  hgvsp: ENST00000406285.3:c.1200C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6270C>T
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20538
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24586
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2533
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6614
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2228
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro479Pro
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP

18-51820061-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820061
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820061
    reference: chr 18
allele count: 1
allele frequency: 1.200768491834774e-5
allele num: 83280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1210G>A
  hgvsp: ENSP00000385196.3:p.Glu404Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.626G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*428G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*542G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1447G>A
  hgvsp: ENSP00000462664.1:p.Glu483Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1069G>A
  hgvsp: ENSP00000217800.5:p.Glu357Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1138G>A
  hgvsp: ENSP00000462681.1:p.Glu380Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.499G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.716G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6280G>A
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26909
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2453
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 403
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Glu483Lys
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: QD

18-51820070-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820070
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820070
    reference: chr 18
allele count: 29
allele frequency: 3.367785390779236e-4
allele num: 86110
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*551C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.725C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.635C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1219C>T
  hgvsp: ENSP00000385196.3:p.Arg407Trp
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1078C>T
  hgvsp: ENSP00000217800.5:p.Arg360Trp
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1147C>T
  hgvsp: ENSP00000462681.1:p.Arg383Trp
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.508C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6289C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1456C>T
  hgvsp: ENSP00000462664.1:p.Arg486Trp
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*437C>T
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6809
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4327
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 691
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16582
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27043
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 862
  bin: 3.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Arg486Trp
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

18-51820071-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820071
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820071
    reference: chr 18
allele count: 8
allele frequency: 9.227646027498385e-5
allele num: 86696
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1457G>A
  hgvsp: ENSP00000462664.1:p.Arg486Gln
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.509G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1079G>A
  hgvsp: ENSP00000217800.5:p.Arg360Gln
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.726G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*438G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*552G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1148G>A
  hgvsp: ENSP00000462681.1:p.Arg383Gln
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6290G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.636G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1220G>A
  hgvsp: ENSP00000385196.3:p.Arg407Gln
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16375
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27097
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 342
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4408
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2732
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6910
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 835
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 846
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Arg486Gln
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum

18-51820081-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820081
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820081
    reference: chr 18
allele count: 3
allele frequency: 3.399818676337262e-5
allele num: 88240
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1467A>G
  hgvsp: ENST00000579534.1:c.1467A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6300A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1230A>G
  hgvsp: ENST00000406285.3:c.1230A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.519A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1089A>G
  hgvsp: ENST00000217800.5:c.1089A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*562A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.646A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1158A>G
  hgvsp: ENST00000579434.1:c.1158A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.736A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*448A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3465
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25220
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 837
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15620
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8414
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 753
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4750
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu489Leu
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ

18-51820106-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820106
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820106
    reference: chr 18
allele count: 1
allele frequency: 1.121151646971769e-5
allele num: 89194
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*587A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1114A>G
  hgvsp: ENSP00000217800.5:p.Arg372Gly
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1255A>G
  hgvsp: ENSP00000385196.3:p.Arg419Gly
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.761A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6325A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*473A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1492A>G
  hgvsp: ENSP00000462664.1:p.Arg498Gly
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1183A>G
  hgvsp: ENSP00000462681.1:p.Arg395Gly
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.544A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.671A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18953
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13006
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 888
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4677
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5732
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14719
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1143
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 851
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg498Gly
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: ReadPosRankSum

18-51820107-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820107
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820107
    reference: chr 18
allele count: 34
allele frequency: 3.813711414213927e-4
allele num: 89152
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.672G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.762G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1184G>A
  hgvsp: ENSP00000462681.1:p.Arg395Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1115G>A
  hgvsp: ENSP00000217800.5:p.Arg372Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*588G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1493G>A
  hgvsp: ENSP00000462664.1:p.Arg498Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1256G>A
  hgvsp: ENSP00000385196.3:p.Arg419Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*474G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.545G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6326G>A
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14682
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13017
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 19002
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4680
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5703
  bin: 1.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 421
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 941
  bin: 4.25e1
  variant carriers: 1
hgvs: p.Arg498Lys
num of homozygotes: 1
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

18-51820115-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820115
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820115
    reference: chr 18
allele count: 1
allele frequency: 1.119820828667413e-5
allele num: 89300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1264G>A
  hgvsp: ENSP00000385196.3:p.Glu422Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1501G>A
  hgvsp: ENSP00000462664.1:p.Glu501Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1192G>A
  hgvsp: ENSP00000462681.1:p.Glu398Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.770G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*482G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.680G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1123G>A
  hgvsp: ENSP00000217800.5:p.Glu375Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.553G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6334G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*596G>A
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1649
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu501Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum

18-51820115-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820115
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820115
    reference: chr 18
allele count: 1
allele frequency: 1.119820828667413e-5
allele num: 89300
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1123G>C
  hgvsp: ENSP00000217800.5:p.Glu375Gln
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*596G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1501G>C
  hgvsp: ENSP00000462664.1:p.Glu501Gln
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.680G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1264G>C
  hgvsp: ENSP00000385196.3:p.Glu422Gln
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1192G>C
  hgvsp: ENSP00000462681.1:p.Glu398Gln
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6334G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.553G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*482G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.770G>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14461
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4618
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6473
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14122
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17272
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4231
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu501Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

18-51820116-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820116
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820116
    reference: chr 18
allele count: 1
allele frequency: 1.120172058428175e-5
allele num: 89272
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1193A>G
  hgvsp: ENSP00000462681.1:p.Glu398Gly
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.771A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*483A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1124A>G
  hgvsp: ENSP00000217800.5:p.Glu375Gly
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6335A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1265A>G
  hgvsp: ENSP00000385196.3:p.Glu422Gly
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1502A>G
  hgvsp: ENSP00000462664.1:p.Glu501Gly
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.554A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*597A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.681A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14439
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16076
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14573
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7229
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1396
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 131
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Glu501Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: European (Finnish)
population: African
population: East Asian
reference allele: A
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum

18-51820118-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820118
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820118
    reference: chr 18
allele count: 2
allele frequency: 2.240996795374583e-5
allele num: 89246
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1504T>A
  hgvsp: ENSP00000462664.1:p.Ser502Thr
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*599T>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1267T>A
  hgvsp: ENSP00000385196.3:p.Ser423Thr
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*485T>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.556T>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.773T>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6337T>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1195T>A
  hgvsp: ENSP00000462681.1:p.Ser399Thr
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1126T>A
  hgvsp: ENSP00000217800.5:p.Ser376Thr
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.683T>A
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7121
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16104
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1258
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14388
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4604
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4376
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1174
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser502Thr
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

18-51820125-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820125
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820125
    reference: chr 18
allele count: 1
allele frequency: 1.126887536623845e-5
allele num: 88740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.563T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*606T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6344T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1133T>C
  hgvsp: ENSP00000217800.5:p.Leu378Pro
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1274T>C
  hgvsp: ENSP00000385196.3:p.Leu425Pro
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462146
  ensembl transcript: ENST00000581950
  gene symbol: POLI
  hgvsc: ENST00000581950.1:c.*492T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1202T>C
  hgvsp: ENSP00000462681.1:p.Leu401Pro
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.690T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1511T>C
  hgvsp: ENSP00000462664.1:p.Leu504Pro
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.780T>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8005
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15173
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14504
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14532
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1490
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Leu504Pro
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: T
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD

18-51820134-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820134
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820134
    reference: chr 18
allele count: 1
allele frequency: 1.134841916521029e-5
allele num: 88118
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.699C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6353C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1211C>T
  hgvsp: ENSP00000462681.1:p.Thr404Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*615C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1283C>T
  hgvsp: ENSP00000385196.3:p.Thr428Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1142C>T
  hgvsp: ENSP00000217800.5:p.Thr381Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1520C>T
  hgvsp: ENSP00000462664.1:p.Thr507Ile
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.789C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.572C>T
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14598
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15406
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13812
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8753
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4736
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1221
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1410
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr507Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: C
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/18-51820136-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820136
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820136
    reference: chr 18
allele count: 0
allele frequency: 0.0e0
allele num: 87898
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1213A>C
  hgvsp: ENSP00000462681.1:p.Asn405His
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*617A>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577727
  gene symbol: POLI
  hgvsc: ENST00000577727.1:n.791A>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1285A>C
  hgvsp: ENSP00000385196.3:p.Asn429His
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.701A>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6355A>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1522A>C
  hgvsp: ENSP00000462664.1:p.Asn508His
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1144A>C
  hgvsp: ENSP00000217800.5:p.Asn382His
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000582366
  gene symbol: POLI
  hgvsc: ENST00000582366.1:n.574A>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8971
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14738
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13528
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 886
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 348
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4007
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1904
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1771
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1394
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn508His
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP

18-51820153-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820153
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820153
    reference: chr 18
allele count: 1
allele frequency: 1.130633380819935e-5
allele num: 88446
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1161A>G
  hgvsp: ENST00000217800.5:c.1161A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*634A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6372A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1302A>G
  hgvsp: ENST00000406285.3:c.1302A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1539A>G
  hgvsp: ENST00000579534.1:c.1539A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1230A>G
  hgvsp: ENST00000579434.1:c.1230A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.718A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8033
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14645
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14945
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14964
  bin: 1.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1595
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18900
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 251
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5802
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 444
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1128
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 849
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys513Lys
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
reference allele: A
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

18-51820154-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820154
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820154
    reference: chr 18
allele count: 1
allele frequency: 1.132220737755033e-5
allele num: 88322
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6373G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.719G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1162G>C
  hgvsp: ENSP00000217800.5:p.Asp388His
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*635G>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1303G>C
  hgvsp: ENSP00000385196.3:p.Asp435His
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1231G>C
  hgvsp: ENSP00000462681.1:p.Asp411His
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1540G>C
  hgvsp: ENSP00000462664.1:p.Asp514His
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14915
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8097
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14961
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14610
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4089
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1389
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1377
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 436
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4643
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1596
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 448
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1544
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 857
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Asp514His
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

18-51820157-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820157
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820157
    reference: chr 18
allele count: 2
allele frequency: 2.248808131690204e-5
allele num: 88936
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1306A>G
  hgvsp: ENSP00000385196.3:p.Ile436Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1165A>G
  hgvsp: ENSP00000217800.5:p.Ile389Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*638A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1543A>G
  hgvsp: ENSP00000462664.1:p.Ile515Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.722A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6376A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1234A>G
  hgvsp: ENSP00000462681.1:p.Ile412Val
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7794
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15352
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14546
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1332
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 943
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14898
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 170
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 597
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18691
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1500
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1416
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5778
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile515Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: MQ

18-51820159-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820159
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820159
    reference: chr 18
allele count: 1
allele frequency: 1.122536033406672e-5
allele num: 89084
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6378T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1167T>C
  hgvsp: ENST00000217800.5:c.1167T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*640T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1236T>C
  hgvsp: ENST00000579434.1:c.1236T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1545T>C
  hgvsp: ENST00000579534.1:c.1545T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1308T>C
  hgvsp: ENST00000406285.3:c.1308T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.724T>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7515
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14793
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15785
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18882
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5674
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1045
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1247
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ile515Ile
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

18-51820162-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820162
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820162
    reference: chr 18
allele count: 1
allele frequency: 1.117518215546913e-5
allele num: 89484
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1239T>C
  hgvsp: ENST00000579434.1:c.1239T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.727T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6381T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1548T>C
  hgvsp: ENST00000579534.1:c.1548T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*643T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1170T>C
  hgvsp: ENST00000217800.5:c.1170T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1311T>C
  hgvsp: ENST00000406285.3:c.1311T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4224
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16489
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14572
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14425
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 952
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16858
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 476
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1284
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 868
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1370
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 306
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asn516Asn
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: ClippingRankSum

18-51820171-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820171
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820171
    reference: chr 18
allele count: 1
allele frequency: 1.101345844622128e-5
allele num: 90798
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1320A>G
  hgvsp: ENST00000406285.3:c.1320A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*652A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1557A>G
  hgvsp: ENST00000579534.1:c.1557A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1248A>G
  hgvsp: ENST00000579434.1:c.1248A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6390A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1179A>G
  hgvsp: ENST00000217800.5:c.1179A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.736A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13800
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13863
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1006
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18476
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4655
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1205
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 522
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1287
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 331
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 812
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2982
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Pro519Pro
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

18-51820174-C-CT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820174
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820175
    reference: chr 18
allele count: 1
allele frequency: 1.093111213134824e-5
allele num: 91482
alternate allele: CT
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1252dupT
  hgvsp: ENSP00000462681.1:p.Cys418LeufsTer5
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*656dupT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.740dupT
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1324dupT
  hgvsp: ENSP00000385196.3:p.Cys442LeufsTer5
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1183dupT
  hgvsp: ENSP00000217800.5:p.Cys395LeufsTer5
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1561dupT
  hgvsp: ENSP00000462664.1:p.Cys521LeufsTer5
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6394dupT
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5669
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4812
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 934
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1039
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 935
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 161
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1975
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4865
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2778
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 585
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Cys521LeufsTer5
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

18-51820181-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820181
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820181
    reference: chr 18
allele count: 1
allele frequency: 1.073721734275345e-5
allele num: 93134
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*662C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1567C>G
  hgvsp: ENSP00000462664.1:p.Leu523Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6400C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1189C>G
  hgvsp: ENSP00000217800.5:p.Leu397Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1330C>G
  hgvsp: ENSP00000385196.3:p.Leu444Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.746C>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1258C>G
  hgvsp: ENSP00000462681.1:p.Leu420Val
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12295
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5047
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4978
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 803
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1134
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13069
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4397
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 176
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 481
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2129
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17334
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 920
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3791
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu523Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: QD

18-51820206-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820206
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820206
    reference: chr 18
allele count: 1
allele frequency: 1.020470641059657e-5
allele num: 97994
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1214T>C
  hgvsp: ENSP00000217800.5:p.Val405Ala
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1355T>C
  hgvsp: ENSP00000385196.3:p.Val452Ala
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1592T>C
  hgvsp: ENSP00000462664.1:p.Val531Ala
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.771T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*687T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1283T>C
  hgvsp: ENSP00000462681.1:p.Val428Ala
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6425T>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5212
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 492
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9785
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10986
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6309
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 509
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 739
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1539
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1453
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3575
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2313
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Val531Ala
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

18-51820209-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820209
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820209
    reference: chr 18
allele count: 2717
allele frequency: 2.741785743117785e-2
allele num: 99096
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1358T>C
  hgvsp: ENSP00000385196.3:p.Phe453Ser
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1217T>C
  hgvsp: ENSP00000217800.5:p.Phe406Ser
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1595T>C
  hgvsp: ENSP00000462664.1:p.Phe532Ser
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6428T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1286T>C
  hgvsp: ENSP00000462681.1:p.Phe429Ser
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.774T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*690T>C
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6705
  bin: 2.75e1
  variant carriers: 362
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 8.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 9575
  bin: 1.25e1
  variant carriers: 382
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 42
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 9.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 7.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 1519
  bin: 3.25e1
  variant carriers: 187
genotype depth: GenotypeDepth
  all individuals: 185
  bin: 5.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 5898
  bin: 1.75e1
  variant carriers: 591
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 454
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24028
  bin: 2.25e1
  variant carriers: 582
genotype depth: GenotypeDepth
  all individuals: 475
  bin: 3.75e1
  variant carriers: 102
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 4.25e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 6.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 10358
  bin: 7.5e0
  variant carriers: 87
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 8.75e1
  variant carriers: 26
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 7.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 9.75e1
  variant carriers: 157
genotype quality: GenotypeQuality
  all individuals: 1013
  bin: 4.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 406
  bin: 8.25e1
  variant carriers: 11
genotype quality: GenotypeQuality
  all individuals: 3402
  bin: 3.25e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 1664
  bin: 4.75e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 2306
  bin: 3.75e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 163
  bin: 8.75e1
  variant carriers: 21
hgvs: p.Phe532Ser
num of homozygotes: 52
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: T
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD

18-51820210-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820210
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820210
    reference: chr 18
allele count: 7
allele frequency: 7.052044085349882e-5
allele num: 99262
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1287C>T
  hgvsp: ENST00000579434.1:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1596C>T
  hgvsp: ENST00000579534.1:c.1596C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1359C>T
  hgvsp: ENST00000406285.3:c.1359C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*691C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.775C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1218C>T
  hgvsp: ENST00000217800.5:c.1218C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6429C>T
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 450
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10285
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1567
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24172
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9540
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 297
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5833
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 452
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3084
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 750
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24554
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3578
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Phe532Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

18-51820221-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820221
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820221
    reference: chr 18
allele count: 2
allele frequency: 1.969007816961033e-5
allele num: 101574
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1229C>T
  hgvsp: ENSP00000217800.5:p.Pro410Leu
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000101751
  ensembl transcript: ENST00000577361
  gene symbol: POLI
  hgvsc: ENST00000577361.1:n.786C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*702C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1607C>T
  hgvsp: ENSP00000462664.1:p.Pro536Leu
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1298C>T
  hgvsp: ENSP00000462681.1:p.Pro433Leu
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6440C>T
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1370C>T
  hgvsp: ENSP00000385196.3:p.Pro457Leu
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5619
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 299
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7731
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 443
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2444
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3100
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12147
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1830
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3279
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro536Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

18-51820229-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820229
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820229
    reference: chr 18
allele count: 1
allele frequency: 9.649529102979774e-6
allele num: 103632
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1615A>G
  hgvsp: ENSP00000462664.1:p.Ile539Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*710A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6448A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1306A>G
  hgvsp: ENSP00000462681.1:p.Ile436Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1237A>G
  hgvsp: ENSP00000217800.5:p.Ile413Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1378A>G
  hgvsp: ENSP00000385196.3:p.Ile460Val
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 477
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8344
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7611
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 220
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11006
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3315
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1069
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1589
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1727
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1725
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3005
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2477
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ile539Val
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: A
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

18-51820230-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820230
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820230
    reference: chr 18
allele count: 1
allele frequency: 9.626121443148127e-6
allele num: 103884
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6449T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1616T>C
  hgvsp: ENSP00000462664.1:p.Ile539Thr
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*711T>C
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1238T>C
  hgvsp: ENSP00000217800.5:p.Ile413Thr
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1307T>C
  hgvsp: ENSP00000462681.1:p.Ile436Thr
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1379T>C
  hgvsp: ENSP00000385196.3:p.Ile460Thr
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7505
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8300
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 476
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27387
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8479
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1035
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 195
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2440
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1485
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3350
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2962
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 137
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28861
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile539Thr
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: African
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

18-51820235-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820235
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820235
    reference: chr 18
allele count: 1
allele frequency: 9.49162838376552e-6
allele num: 105356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*716G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1384G>A
  hgvsp: ENSP00000385196.3:p.Glu462Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1621G>A
  hgvsp: ENSP00000462664.1:p.Glu541Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6454G>A
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1312G>A
  hgvsp: ENSP00000462681.1:p.Glu438Lys
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1243G>A
  hgvsp: ENSP00000217800.5:p.Glu415Lys
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 284
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6672
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9102
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7525
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1953
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29034
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31005
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2013
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1222
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1591
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 992
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9865
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 892
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu541Lys
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: QD

18-51820241-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 51820241
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 51820241
    reference: chr 18
allele count: 1
allele frequency: 9.303017899006437e-6
allele num: 107492
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000385196
  ensembl transcript: ENST00000406285
  gene symbol: POLI
  hgvsc: ENST00000406285.3:c.1390A>G
  hgvsp: ENSP00000385196.3:p.Ile464Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462664
  ensembl transcript: ENST00000579534
  gene symbol: POLI
  hgvsc: ENST00000579534.1:c.1627A>G
  hgvsp: ENSP00000462664.1:p.Ile543Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463065
  ensembl transcript: ENST00000579823
  gene symbol: POLI
  hgvsc: ENST00000579823.1:c.333+6460A>G
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000462681
  ensembl transcript: ENST00000579434
  gene symbol: POLI
  hgvsc: ENST00000579434.1:c.1318A>G
  hgvsp: ENSP00000462681.1:p.Ile440Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000217800
  ensembl transcript: ENST00000217800
  gene symbol: POLI
  hgvsc: ENST00000217800.5:c.1249A>G
  hgvsp: ENSP00000217800.5:p.Ile417Val
  variant of: http://identifiers.org/hgnc/9182
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101751
  ensembl protein: ENSP00000463971
  ensembl transcript: ENST00000585023
  gene symbol: POLI
  hgvsc: ENST00000585023.1:c.*722A>G
  variant of: http://identifiers.org/hgnc/9182
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5635
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ile543Val
num of homozygotes: 0
reference allele: A

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1426
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5454
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1211
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 10
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 14
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2381
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 48271
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.637625289128758e-5
allele num: 10376
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: 11460
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8642
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -8.712e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.46e-1

FS
type: SiteQuality
SIO_000300: 1.0583e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.405e0

MQRankSum
type: SiteQuality
SIO_000300: -1.71e0

DP
type: SiteQuality
SIO_000300: 1.447376e6

QD
type: SiteQuality
SIO_000300: 1.607e1

GenotypeQuality
all individuals: 857
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 9.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1423
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5454
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66598
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.065752759917505e-5
allele num: 16486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.289e1

FS
type: SiteQuality
SIO_000300: 6.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 1.446397e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.28e-1

GenotypeQuality
all individuals: 1423
bin: 7.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 27
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5454
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 432
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48199
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2383
bin: 9.75e1
variant carriers: 1

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11460
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10352
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50154659299078e-5
allele num: 66598
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

FS
type: SiteQuality
SIO_000300: 6.42e-1

QD
type: SiteQuality
SIO_000300: 1.289e1

MQRankSum
type: SiteQuality
SIO_000300: 5.1e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.446397e6

VQSLOD
type: SiteQuality
SIO_000300: 1.05e0

GenotypeQuality
all individuals: 387
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48149
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5444
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 23
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 431
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 7
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1424
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2412
bin: 9.75e1
variant carriers: 31

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

GenotypeQuality
all individuals: 1208
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.473830477072719e-4
allele num: 8636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.501681883709755e-5
allele num: 66592
num of homozygotes: 0

South Asian
type: Population
allele count: 26
allele frequency: 1.577861390945503e-3
allele num: 16478
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.722958827634333e-5
allele num: 11464
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10342
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 1.97e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.49e-1

MQ
type: SiteQuality
SIO_000300: 5.996e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -2.84e-1

QD
type: SiteQuality
SIO_000300: 1.296e1

VQSLOD
type: SiteQuality
SIO_000300: 5.74e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.68e-1

DP
type: SiteQuality
SIO_000300: 1.447485e6

GenotypeQuality
all individuals: 377
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2419
bin: 9.75e1
variant carriers: 35

GenotypeQuality
all individuals: 12
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1424
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 855
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 432
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 383
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 47952
bin: 6.25e1
variant carriers: 0

South Asian
type: Population
allele count: 5
allele frequency: 3.03951367781155e-4
allele num: 16450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.010518407212622e-5
allele num: 66550
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.491620111731844e-4
allele num: 11456
num of homozygotes: 0

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

East Asian
type: Population
allele count: 21
allele frequency: 2.432244614315497e-3
allele num: 8634
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.85e0

VQSLOD
type: SiteQuality
SIO_000300: 3.04e0

DP
type: SiteQuality
SIO_000300: 1.447792e6

MQRankSum
type: SiteQuality
SIO_000300: 3.67e-1

FS
type: SiteQuality
SIO_000300: 1.127e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
SIO_000300: 1.367e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.02e-1

GenotypeQuality
all individuals: 33
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 856
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 7.25e1
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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2403
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5432
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.087168249330411e-5
allele num: 16428
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11458
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66540
num of homozygotes: 0

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

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

QD
type: SiteQuality
SIO_000300: 1.099e1

MQRankSum
type: SiteQuality
SIO_000300: -7.82e-1

VQSLOD
type: SiteQuality
SIO_000300: 5.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 2.011e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.163e0

DP
type: SiteQuality
SIO_000300: 1.444461e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.34e0

GenotypeQuality
all individuals: 47810
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
all individuals: 16
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 22
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variant carriers: 0

GenotypeQuality
all individuals: 434
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GenotypeQuality
all individuals: 2404
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 8.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10270
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.503262078710802e-5
allele num: 66522
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 1.913e0

VQSLOD
type: SiteQuality
SIO_000300: -7.853e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e0

DP
type: SiteQuality
SIO_000300: 1.443806e6

QD
type: SiteQuality
SIO_000300: 9.279999999999999e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.708e0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e-1

MQ
type: SiteQuality
SIO_000300: 5.909e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-2

GenotypeQuality
all individuals: 25
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
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variant carriers: 0

GenotypeQuality
all individuals: 5
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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: 4
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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
all individuals: 18
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variant carriers: 0

GenotypeQuality
all individuals: 30
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variant carriers: 0

GenotypeQuality
all individuals: 385
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variant carriers: 0

GenotypeQuality
all individuals: 12
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variant carriers: 0

GenotypeQuality
all individuals: 47681
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1420
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variant carriers: 0

GenotypeQuality
all individuals: 2408
bin: 9.75e1
variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16378
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10240
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.730574471800244e-5
allele num: 11454
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66474
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.0e-1

InbreedingCoeff
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SIO_000300: 4.0e-4

ReadPosRankSum
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SIO_000300: -1.259e0

BaseQRankSum
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SIO_000300: 7.0e-1

DP
type: SiteQuality
SIO_000300: 1.442454e6

FS
type: SiteQuality
SIO_000300: 1.171e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.32e0

QD
type: SiteQuality
SIO_000300: 8.77e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -4.187e-1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 15

GenotypeQuality
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variant carriers: 0

Other
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allele frequency: 0.0e0
allele num: 902
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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11452
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

European (Non-Finnish)
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allele count: 15
allele frequency: 2.257676098735701e-4
allele num: 66440
num of homozygotes: 0

ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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VQSLOD
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FS
type: SiteQuality
SIO_000300: 5.629999999999999e-1

MQ
type: SiteQuality
SIO_000300: 5.951e1

QD
type: SiteQuality
SIO_000300: 1.176e1

DP
type: SiteQuality
SIO_000300: 1.442258e6

BaseQRankSum
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MQRankSum
type: SiteQuality
SIO_000300: 3.74e-1

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

Other
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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: 6610
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

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

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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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: 3.009691205682297e-5
allele num: 66452
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.182e0

BaseQRankSum
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InbreedingCoeff
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SIO_000300: 2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.9e-2

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 8.3e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

DP
type: SiteQuality
SIO_000300: 1.441681e6

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10208
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66436
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16350
num of homozygotes: 0

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

East Asian
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allele count: 16
allele frequency: 1.853138753764188e-3
allele num: 8634
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.56e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
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SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.139999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.71e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

QD
type: SiteQuality
SIO_000300: 1.388e1

DP
type: SiteQuality
SIO_000300: 1.443456e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 0
allele frequency: 0.0e0
allele num: 10204
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16320
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66436
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.733624454148471e-5
allele num: 11450
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
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MQ
type: SiteQuality
SIO_000300: 5.844e1

BaseQRankSum
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VQSLOD
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DP
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MQRankSum
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ClippingRankSum
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QD
type: SiteQuality
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InbreedingCoeff
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FS
type: SiteQuality
SIO_000300: 7.185e0

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11432
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.017410458344649e-5
allele num: 66282
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.33e-1

MQRankSum
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VQSLOD
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MQ
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BaseQRankSum
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DP
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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East Asian
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66184
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South Asian
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African
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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MQ
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BaseQRankSum
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DP
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FS
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ClippingRankSum
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QD
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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num of homozygotes: 0

African
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South Asian
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East Asian
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Other
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European (Finnish)
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European (Non-Finnish)
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allele frequency: 4.604051565377532e-5
allele num: 65160
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QD
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InbreedingCoeff
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MQRankSum
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DP
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MQ
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VQSLOD
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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FS
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1022
bin: 7.25e1
variant carriers: 9

GenotypeQuality
all individuals: 78
bin: 4.75e1
variant carriers: 5

GenotypeQuality
all individuals: 346
bin: 8.75e1
variant carriers: 11

Other
type: Population
allele count: 43
allele frequency: 4.809843400447427e-2
allele num: 894
num of homozygotes: 3

East Asian
type: Population
allele count: 30
allele frequency: 3.479471120389701e-3
allele num: 8622
num of homozygotes: 0

African
type: Population
allele count: 902
allele frequency: 9.151785714285714e-2
allele num: 9856
num of homozygotes: 51

European (Finnish)
type: Population
allele count: 441
allele frequency: 6.685870224378411e-2
allele num: 6596
num of homozygotes: 12

European (Non-Finnish)
type: Population
allele count: 4568
allele frequency: 6.925619333515268e-2
allele num: 65958
num of homozygotes: 145

Latino
type: Population
allele count: 338
allele frequency: 2.96127562642369e-2
allele num: 11414
num of homozygotes: 4

South Asian
type: Population
allele count: 453
allele frequency: 2.890874282067645e-2
allele num: 15670
num of homozygotes: 10

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.97e-1

DP
type: SiteQuality
SIO_000300: 1.695563e6

FS
type: SiteQuality
SIO_000300: 3.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.01e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.23e0

QD
type: SiteQuality
SIO_000300: 1.363e1

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.12e0

MQ
type: SiteQuality
SIO_000300: 5.851e1

GenotypeQuality
all individuals: 456
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6080
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 2107
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 750
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39486
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 333
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2305
bin: 9.75e1
variant carriers: 125

GenotypeQuality
all individuals: 1215
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 5.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 1007
bin: 7.25e1
variant carriers: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8550
num of homozygotes: 0

African
type: Population
allele count: 115
allele frequency: 1.410696761530913e-2
allele num: 8152
num of homozygotes: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14640
num of homozygotes: 0

Latino
type: Population
allele count: 6
allele frequency: 5.585552038726494e-4
allele num: 10742
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 7.011147724882563e-5
allele num: 57052
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5736
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.240694789081886e-3
allele num: 806
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.179e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.44e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.32e-1

DP
type: SiteQuality
SIO_000300: 1.694857e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.7e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.55e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.74e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.58e-1

GenotypeQuality
all individuals: 978
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 428
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1544
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 822
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 537
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5428
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1236
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2940
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3068
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 363
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9760
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65738
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

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

South Asian
type: Population
allele count: 3
allele frequency: 1.954652071931196e-4
allele num: 15348
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 6.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.09e-1

MQRankSum
type: SiteQuality
SIO_000300: -2.49e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
SIO_000300: 1.638e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.65e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.28e0

DP
type: SiteQuality
SIO_000300: 1.531602e6

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

GenotypeQuality
all individuals: 64
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 86
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3039
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1534
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3181
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 974
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41023
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5363
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6594
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9732
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.162250116225012e-4
allele num: 8604
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15206
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65632
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.521303e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.038e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

MQ
type: SiteQuality
SIO_000300: 5.946e1

MQRankSum
type: SiteQuality
SIO_000300: -3.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.2e-1

QD
type: SiteQuality
SIO_000300: 2.551e1

VQSLOD
type: SiteQuality
SIO_000300: -1.618e0

GenotypeQuality
all individuals: 922
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1499
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1045
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3040
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 5101
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 92
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 39520
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1188
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 968
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1506
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11352
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9622
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65386
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.663113006396588e-5
allele num: 15008
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8590
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.545e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.003e0

VQSLOD
type: SiteQuality
SIO_000300: -2.582e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.01e0

DP
type: SiteQuality
SIO_000300: 1.499849e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.23e-1

GenotypeQuality
all individuals: 108
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1694
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3040
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1305
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3129
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4822
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 223
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 425
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1483
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1162
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 541
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38286
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9496
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 868
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6556
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.348617666891436e-4
allele num: 14830
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65018
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11336
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.485523e6

FS
type: SiteQuality
SIO_000300: 7.683e0

MQRankSum
type: SiteQuality
SIO_000300: -2.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.12e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.2e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.93e-1

MQ
type: SiteQuality
SIO_000300: 5.979e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.13e0

QD
type: SiteQuality
SIO_000300: 1.6e1

GenotypeQuality
all individuals: 1746
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 399
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1165
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1481
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1200
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4719
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 965
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 427
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 668
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36001
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 764
bin: 4.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9432
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.544306143249838e-5
allele num: 64754
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11318
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.0e-2

MQ
type: SiteQuality
SIO_000300: 5.548e1

DP
type: SiteQuality
SIO_000300: 1.471395e6

MQRankSum
type: SiteQuality
SIO_000300: -3.7e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 4.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.085e0

QD
type: SiteQuality
SIO_000300: 1.794e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.138e0

GenotypeQuality
all individuals: 966
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1196
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1473
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 277
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3038
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1963
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1147
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2830
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 423
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1816
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4703
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35644
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 798
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1250
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.060895395713983e-4
allele num: 9426
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14376
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 860
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.41e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.438e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.2e-1

DP
type: SiteQuality
SIO_000300: 1.470344e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.99e-1

QD
type: SiteQuality
SIO_000300: 8.0e0

MQ
type: SiteQuality
SIO_000300: 5.835e1

GenotypeQuality
all individuals: 308
bin: 1.75e1
variant carriers: 11

GenotypeQuality
all individuals: 372
bin: 2.5e0
variant carriers: 3

GenotypeQuality
all individuals: 572
bin: 4.25e1
variant carriers: 9

GenotypeQuality
all individuals: 2468
bin: 2.25e1
variant carriers: 7

GenotypeQuality
all individuals: 1030
bin: 2.75e1
variant carriers: 8

GenotypeQuality
all individuals: 1007
bin: 7.25e1
variant carriers: 16

GenotypeQuality
all individuals: 4338
bin: 6.75e1
variant carriers: 26

GenotypeQuality
all individuals: 1361
bin: 3.75e1
variant carriers: 19

GenotypeQuality
all individuals: 297
bin: 1.25e1
variant carriers: 14

GenotypeQuality
all individuals: 543
bin: 7.5e0
variant carriers: 8

GenotypeQuality
all individuals: 332
bin: 5.25e1
variant carriers: 15

GenotypeQuality
all individuals: 779
bin: 8.25e1
variant carriers: 29

GenotypeQuality
all individuals: 416
bin: 9.25e1
variant carriers: 27

GenotypeQuality
all individuals: 8216
bin: 9.75e1
variant carriers: 5975

GenotypeQuality
all individuals: 802
bin: 4.75e1
variant carriers: 15

GenotypeQuality
all individuals: 1226
bin: 7.75e1
variant carriers: 21

GenotypeQuality
all individuals: 372
bin: 8.75e1
variant carriers: 37

European (Finnish)
type: Population
allele count: 436
allele frequency: 6.636225266362253e-2
allele num: 6570
num of homozygotes: 12

East Asian
type: Population
allele count: 30
allele frequency: 3.50385423966363e-3
allele num: 8562
num of homozygotes: 0

South Asian
type: Population
allele count: 333
allele frequency: 2.31636060100167e-2
allele num: 14376
num of homozygotes: 5

Latino
type: Population
allele count: 318
allele frequency: 2.813661298885153e-2
allele num: 11302
num of homozygotes: 3

African
type: Population
allele count: 839
allele frequency: 8.822292323869611e-2
allele num: 9510
num of homozygotes: 41

European (Non-Finnish)
type: Population
allele count: 4320
allele frequency: 6.659267480577137e-2
allele num: 64872
num of homozygotes: 113

Other
type: Population
allele count: 41
allele frequency: 4.745370370370371e-2
allele num: 864
num of homozygotes: 3

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.92e-1

DP
type: SiteQuality
SIO_000300: 1.461675e6

VQSLOD
type: SiteQuality
SIO_000300: 5.62e0

MQRankSum
type: SiteQuality
SIO_000300: -5.81e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-2

MQ
type: SiteQuality
SIO_000300: 5.78e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.4e-3

QD
type: SiteQuality
SIO_000300: 1.185e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.5e-1

GenotypeQuality
all individuals: 1450
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1590
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 346
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1045
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 766
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 667
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2387
bin: 9.75e1
variant carriers: 108

GenotypeQuality
all individuals: 493
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2382
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 375
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1059
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1005
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4308
bin: 6.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5742
num of homozygotes: 0

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

Latino
type: Population
allele count: 8
allele frequency: 7.483629560336763e-4
allele num: 10690
num of homozygotes: 0

African
type: Population
allele count: 101
allele frequency: 1.264713248184323e-2
allele num: 7986
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 56716
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8500
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13718
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.79e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e0

MQRankSum
type: SiteQuality
SIO_000300: 4.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.22616e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.701e1

GenotypeQuality
all individuals: 600
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1285
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 682
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 523
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1866
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2467
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1551
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4765
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variant carriers: 0

GenotypeQuality
all individuals: 1789
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1029
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1883
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33018
bin: 6.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14090
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.558554907889405e-5
allele num: 64162
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11250
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 852
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e-1

FS
type: SiteQuality
SIO_000300: 1.2923e1

MQRankSum
type: SiteQuality
SIO_000300: -2.7e-1

QD
type: SiteQuality
SIO_000300: 1.356e1

VQSLOD
type: SiteQuality
SIO_000300: -1.546e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.215e0

DP
type: SiteQuality
SIO_000300: 1.431117e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

GenotypeQuality
all individuals: 1028
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32085
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 200
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2027
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1897
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variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2306
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1848
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1673
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1265
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 431
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1113
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 634
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 433
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4932
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1326
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9486
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8544
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 856
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11280
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 4.27960057061341e-4
allele num: 14020
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64700
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.6e-2

FS
type: SiteQuality
SIO_000300: 6.696e0

MQRankSum
type: SiteQuality
SIO_000300: -1.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

QD
type: SiteQuality
SIO_000300: 1.244e1

DP
type: SiteQuality
SIO_000300: 1.431935e6

GenotypeQuality
all individuals: 557
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2033
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7035
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12177
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10975
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1912
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13628
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3724
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 154
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4135
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1474
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1696
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3158
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1904
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16106
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2780
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 256
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.47e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.370000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.56e-2

QD
type: SiteQuality
SIO_000300: 8.15e0

DP
type: SiteQuality
SIO_000300: 4.85442e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

GenotypeQuality
all individuals: 23299
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4708
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 282
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 7.25e1
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GenotypeQuality
all individuals: 5344
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11433
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 496
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1238
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 489
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4250
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1989
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3781
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1143
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 170
bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1784
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 1.804402742692169e-4
allele num: 16626
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3222
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2818
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1990
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 5.14076e5

VQSLOD
type: SiteQuality
SIO_000300: -7.140000000000001e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.21e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.712e1

GenotypeQuality
all individuals: 158
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3778
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4280
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11085
bin: 7.5e0
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GenotypeQuality
all individuals: 4742
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 710
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 126
bin: 5.25e1
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GenotypeQuality
all individuals: 93
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24603
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1955
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1405
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 461
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.943889681407513e-5
allele num: 16824
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1590
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1814
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2840
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2016
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3260
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.27e-1

QD
type: SiteQuality
SIO_000300: 1.403e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.09e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.58e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.51e-1

DP
type: SiteQuality
SIO_000300: 5.23122e5

GenotypeQuality
all individuals: 44
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4496
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 95
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GenotypeQuality
all individuals: 711
bin: 2.5e0
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GenotypeQuality
all individuals: 3791
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1142
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 418
bin: 4.75e1
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GenotypeQuality
all individuals: 1541
bin: 6.25e1
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GenotypeQuality
all individuals: 3747
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4262
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variant carriers: 0

GenotypeQuality
all individuals: 25502
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 453
bin: 4.25e1
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GenotypeQuality
all individuals: 128
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1816
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2024
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16950
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 258
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1612
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.47e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 7.97e0

MQRankSum
type: SiteQuality
SIO_000300: 7.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 5.27383e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.05e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.36e-1

GenotypeQuality
all individuals: 362
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 340
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4282
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27549
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1834
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1940
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10032
bin: 7.5e0
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GenotypeQuality
all individuals: 3515
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3448
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 166
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 9.75e1
variant carriers: 2

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2908
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2112
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3372
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1684
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1876
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 274
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 17486
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.033e1

DP
type: SiteQuality
SIO_000300: 5.43122e5

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.62e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.305e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.5e-1

MQ
type: SiteQuality
SIO_000300: 5.728e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

GenotypeQuality
all individuals: 431
bin: 4.25e1
variant carriers: 205

GenotypeQuality
all individuals: 886
bin: 9.25e1
variant carriers: 811

GenotypeQuality
all individuals: 13365
bin: 9.75e1
variant carriers: 12682

GenotypeQuality
all individuals: 507
bin: 4.75e1
variant carriers: 321

GenotypeQuality
all individuals: 2827
bin: 2.75e1
variant carriers: 643

GenotypeQuality
all individuals: 418
bin: 5.25e1
variant carriers: 351

GenotypeQuality
all individuals: 361
bin: 8.25e1
variant carriers: 266

GenotypeQuality
all individuals: 309
bin: 7.75e1
variant carriers: 214

GenotypeQuality
all individuals: 2208
bin: 1.25e1
variant carriers: 297

GenotypeQuality
all individuals: 2308
bin: 1.75e1
variant carriers: 772

GenotypeQuality
all individuals: 4230
bin: 2.5e0
variant carriers: 45

GenotypeQuality
all individuals: 551
bin: 6.75e1
variant carriers: 363

GenotypeQuality
all individuals: 1786
bin: 6.25e1
variant carriers: 552

GenotypeQuality
all individuals: 333
bin: 7.25e1
variant carriers: 247

GenotypeQuality
all individuals: 502
bin: 5.75e1
variant carriers: 462

GenotypeQuality
all individuals: 17343
bin: 2.25e1
variant carriers: 933

GenotypeQuality
all individuals: 2963
bin: 3.25e1
variant carriers: 691

Latino
type: Population
allele count: 750
allele frequency: 2.765486725663717e-1
allele num: 2712
num of homozygotes: 55

East Asian
type: Population
allele count: 105
allele frequency: 4.725472547254726e-2
allele num: 2222
num of homozygotes: 2

Other
type: Population
allele count: 112
allele frequency: 3.2e-1
allele num: 350
num of homozygotes: 15

African
type: Population
allele count: 1270
allele frequency: 2.991050400376825e-1
allele num: 4246
num of homozygotes: 137

South Asian
type: Population
allele count: 1147
allele frequency: 4.016106442577031e-1
allele num: 2856
num of homozygotes: 167

European (Finnish)
type: Population
allele count: 1026
allele frequency: 2.951668584579977e-1
allele num: 3476
num of homozygotes: 122

European (Non-Finnish)
type: Population
allele count: 9729
allele frequency: 3.824292452830189e-1
allele num: 25440
num of homozygotes: 1363

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 5.87e0

DP
type: SiteQuality
SIO_000300: 6.14007e5

MQRankSum
type: SiteQuality
SIO_000300: 1.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.82e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.981e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

GenotypeQuality
all individuals: 3078
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2530
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3834
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 97
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5504
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 584
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 213
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GenotypeQuality
all individuals: 25260
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2789
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6882
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 5.75e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 3.35795836131632e-4
allele num: 2978
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2400
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3596
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26534
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4398
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.164e0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.18e-2

MQRankSum
type: SiteQuality
SIO_000300: -7.41e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.38e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.65e-1

DP
type: SiteQuality
SIO_000300: 6.26063e5

QD
type: SiteQuality
SIO_000300: 6.28e0

GenotypeQuality
all individuals: 1388
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 212
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 381
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 997
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6086
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4443
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27459
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2960
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2222
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5293
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 494
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3576
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4488
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2526
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2950
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26984
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3662
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3072
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.29e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.24e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 6.4675e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

FS
type: SiteQuality
SIO_000300: 3.01e0

MQRankSum
type: SiteQuality
SIO_000300: 1.13e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.53e-1

QD
type: SiteQuality
SIO_000300: 1.346e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.13e-1

GenotypeQuality
all individuals: 450
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1547
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3420
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14627
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 285
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2263
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1399
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 114
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3392
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 260
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 212
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4588
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5642
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4260
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4662
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.947591817485115e-5
allele num: 33926
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4338
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.11e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.4e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -1.33e-1

DP
type: SiteQuality
SIO_000300: 8.14707e5

QD
type: SiteQuality
SIO_000300: 1.354e1

GenotypeQuality
all individuals: 212
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2911
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 658
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 365
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27088
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1712
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17338
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 457
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 812
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3020
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1024
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 224
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 487
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 8.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1439
bin: 9.75e1
variant carriers: 38

European (Non-Finnish)
type: Population
allele count: 26
allele frequency: 7.054099517065494e-4
allele num: 36858
num of homozygotes: 0

Latino
type: Population
allele count: 9
allele frequency: 1.67973124300112e-3
allele num: 5358
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 506
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6072
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.621876131836291e-4
allele num: 5522
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4848
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4564
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

FS
type: SiteQuality
SIO_000300: 1.339e0

QD
type: SiteQuality
SIO_000300: 1.217e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.399999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.01e0

DP
type: SiteQuality
SIO_000300: 8.73239e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.4e-1

GenotypeQuality
all individuals: 315
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2830
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1402
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 182
bin: 2.5e0
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GenotypeQuality
all individuals: 115
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GenotypeQuality
all individuals: 160
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GenotypeQuality
all individuals: 1059
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variant carriers: 0

GenotypeQuality
all individuals: 1597
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GenotypeQuality
all individuals: 468
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variant carriers: 0

GenotypeQuality
all individuals: 26640
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2916
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 948
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1306
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6174
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4994
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.660989888238425e-5
allele num: 37580
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5820
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5522
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4628
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 518
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.269e1

MQ
type: SiteQuality
SIO_000300: 5.922e1

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-1

DP
type: SiteQuality
SIO_000300: 8.86902e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.64e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.12e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.53e-1

GenotypeQuality
all individuals: 1120
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 2.5e0
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GenotypeQuality
all individuals: 238
bin: 8.25e1
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GenotypeQuality
all individuals: 315
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2811
bin: 2.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 746
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 646
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GenotypeQuality
all individuals: 1207
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 769
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GenotypeQuality
all individuals: 2705
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25699
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1454
bin: 7.5e0
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GenotypeQuality
all individuals: 329
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GenotypeQuality
all individuals: 117
bin: 8.75e1
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GenotypeQuality
all individuals: 314
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1441
bin: 9.75e1
variant carriers: 42

GenotypeQuality
all individuals: 162
bin: 9.25e1
variant carriers: 2

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4768
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 532
num of homozygotes: 0

African
type: Population
allele count: 41
allele frequency: 6.462799495586381e-3
allele num: 6344
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 38842
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.728309713100588e-4
allele num: 5786
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5178
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.46e0

MQRankSum
type: SiteQuality
SIO_000300: 3.18e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.162e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

DP
type: SiteQuality
SIO_000300: 9.08106e5

QD
type: SiteQuality
SIO_000300: 1.193e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.54e-1

GenotypeQuality
all individuals: 253
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1295
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8198
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5092
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6804
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.319217032329885e-5
allele num: 43118
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6690
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 614
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5808
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.475e0

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 9.399999999999999e-1

DP
type: SiteQuality
SIO_000300: 9.85527e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.737e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.057e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.29e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 4.53e-1

QD
type: SiteQuality
SIO_000300: 9.960000000000001e0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 6834
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6860
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5138
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 618
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5920
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 43744
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.257e0

VQSLOD
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ClippingRankSum
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SIO_000300: 2.03e-1

FS
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 9.97541e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 10120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.154522342396691e-5
allele num: 46414
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7128
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5314
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7390
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

FS
type: SiteQuality
SIO_000300: 4.658e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.35e-1

VQSLOD
type: SiteQuality
SIO_000300: -6.395e-1

MQ
type: SiteQuality
SIO_000300: 5.89e1

DP
type: SiteQuality
SIO_000300: 1.044613e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.53e0

QD
type: SiteQuality
SIO_000300: 1.305e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 28

GenotypeQuality
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variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 1.374759417102007e-4
allele num: 7274
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6386
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11112
num of homozygotes: 0

Latino
type: Population
allele count: 24
allele frequency: 3.154574132492113e-3
allele num: 7608
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5400
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 8.394543546694649e-5
allele num: 47650
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.04e0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.47e0

MQRankSum
type: SiteQuality
SIO_000300: 2.31e-1

DP
type: SiteQuality
SIO_000300: 1.067208e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e-1

QD
type: SiteQuality
SIO_000300: 1.061e1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 7

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: 680
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7294
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.312680493567866e-4
allele num: 7618
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5424
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47934
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 6.167400881057269e-4
allele num: 11350
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

MQRankSum
type: SiteQuality
SIO_000300: 3.82e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.89e-1

DP
type: SiteQuality
SIO_000300: 1.069773e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.68e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.45e-1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11964
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48516
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5474
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7684
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6484
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 4.038772213247173e-4
allele num: 7428
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.075e0

MQRankSum
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SIO_000300: 1.9e0

BaseQRankSum
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SIO_000300: 3.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

FS
type: SiteQuality
SIO_000300: 1.0611e1

DP
type: SiteQuality
SIO_000300: 1.063909e6

QD
type: SiteQuality
SIO_000300: 1.751e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.3e-3

MQ
type: SiteQuality
SIO_000300: 5.935e1

GenotypeQuality
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12516
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.31578947368421e-4
allele num: 7600
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7636
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48858
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5520
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.26e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.08e-1

FS
type: SiteQuality
SIO_000300: 1.906e0

VQSLOD
type: SiteQuality
SIO_000300: -3.06e-2

QD
type: SiteQuality
SIO_000300: 1.226e1

DP
type: SiteQuality
SIO_000300: 1.016208e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.52e-1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1437
bin: 9.75e1
variant carriers: 29

GenotypeQuality
all individuals: 169
bin: 9.25e1
variant carriers: 1

African
type: Population
allele count: 29
allele frequency: 3.81578947368421e-3
allele num: 7600
num of homozygotes: 1

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6368
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12518
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5516
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 6.546216286986122e-4
allele num: 7638
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.637e0

MQRankSum
type: SiteQuality
SIO_000300: 2.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

QD
type: SiteQuality
SIO_000300: 1.289e1

FS
type: SiteQuality
SIO_000300: 2.45e0

VQSLOD
type: SiteQuality
SIO_000300: 3.03e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-1

DP
type: SiteQuality
SIO_000300: 1.017212e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 131
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
all individuals: 284
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 420
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.047250542521394e-5
allele num: 48846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5524
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7650
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7656
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.003419e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

FS
type: SiteQuality
SIO_000300: 5.543e0

MQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

QD
type: SiteQuality
SIO_000300: 1.236e1

MQ
type: SiteQuality
SIO_000300: 5.948e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.179e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 169
bin: 9.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7650
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.932730445819452e-5
allele num: 12606
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7656
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48846
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5524
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.003419e6

VQSLOD
type: SiteQuality
SIO_000300: 1.56e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.179e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.8e-1

MQ
type: SiteQuality
SIO_000300: 5.948e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.6e-3

FS
type: SiteQuality
SIO_000300: 5.543e0

MQRankSum
type: SiteQuality
SIO_000300: -1.92e-1

QD
type: SiteQuality
SIO_000300: 1.236e1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.1e-2

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.047669751822426e-5
allele num: 48836
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7640
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12584
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5538
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7652
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

MQRankSum
type: SiteQuality
SIO_000300: 3.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.93e-1

QD
type: SiteQuality
SIO_000300: 1.167e1

FS
type: SiteQuality
SIO_000300: 3.703e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.47e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.6e-3

DP
type: SiteQuality
SIO_000300: 9.9294e5

BaseQRankSum
type: SiteQuality
SIO_000300: 1.75e0

GenotypeQuality
all individuals: 858
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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: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 19696
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GenotypeQuality
all individuals: 286
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 694
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 3.161555485298767e-4
allele num: 6326
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12598
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48790
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5544
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 1.31e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

VQSLOD
type: SiteQuality
SIO_000300: 2.77e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.513e0

DP
type: SiteQuality
SIO_000300: 9.94196e5

QD
type: SiteQuality
SIO_000300: 1.218e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 170
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GenotypeQuality
all individuals: 15433
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5512
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12610
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7666
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48424
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.592863969417012e-4
allele num: 6278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7562
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 688
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.22e-1

DP
type: SiteQuality
SIO_000300: 9.80283e5

QD
type: SiteQuality
SIO_000300: 1.326e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.99e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.139e0

VQSLOD
type: SiteQuality
SIO_000300: 1.07e0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.081772004330086e-5
allele num: 48036
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7702
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7426
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12560
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5502
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

DP
type: SiteQuality
SIO_000300: 9.68698e5

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.992e0

VQSLOD
type: SiteQuality
SIO_000300: 1.02e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.71e-1

QD
type: SiteQuality
SIO_000300: 1.589e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.53e-1

GenotypeQuality
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variant carriers: 1

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7684
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12540
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5478
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 47910
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6204
num of homozygotes: 0

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

FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.27e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.291e1

DP
type: SiteQuality
SIO_000300: 9.64954e5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1413
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5524
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12650
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6204
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.074860984314051e-5
allele num: 48196
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -8.463000000000001e-1

DP
type: SiteQuality
SIO_000300: 9.79485e5

MQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -4.5e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.65e-1

FS
type: SiteQuality
SIO_000300: 1.585e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -9.379999999999999e-1

QD
type: SiteQuality
SIO_000300: 6.57e0

GenotypeQuality
all individuals: 1413
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 14545
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1592
bin: 4.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12630
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6180
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7406
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.466275659824047e-3
allele num: 682
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48142
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7768
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.73e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.36e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.03e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.2e0

DP
type: SiteQuality
SIO_000300: 9.79737e5

GenotypeQuality
all individuals: 1220
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 15055
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variant carriers: 0

GenotypeQuality
all individuals: 3682
bin: 3.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.061430632859204e-5
allele num: 48510
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7462
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5578
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.877737513786041e-5
allele num: 12694
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7812
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6196
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.25e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.1e-3

DP
type: SiteQuality
SIO_000300: 9.84387e5

ClippingRankSum
type: SiteQuality
SIO_000300: -8.090000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.159e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.63e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 706
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12716
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6216
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7474
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.058206067591487e-5
allele num: 48586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5584
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.025e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.4e-3

DP
type: SiteQuality
SIO_000300: 9.88783e5

MQRankSum
type: SiteQuality
SIO_000300: 3.42e-1

FS
type: SiteQuality
SIO_000300: 2.062e0

VQSLOD
type: SiteQuality
SIO_000300: 2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.3e-1

QD
type: SiteQuality
SIO_000300: 1.027e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.27e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1154
bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3418
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GenotypeQuality
all individuals: 388
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 696
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6238
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48836
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.327316166710911e-4
allele num: 7534
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5600
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7822
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12758
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -8.371e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.85e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.54e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-2

MQ
type: SiteQuality
SIO_000300: 5.79e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

DP
type: SiteQuality
SIO_000300: 9.95688e5

QD
type: SiteQuality
SIO_000300: 1.493e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.57e-1

GenotypeQuality
all individuals: 4225
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
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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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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1874
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variant carriers: 0

GenotypeQuality
all individuals: 706
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7680
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 702
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49530
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.25281884239539e-4
allele num: 7982
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12912
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5664
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.024034e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.34e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.159e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -7.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.96e-1

QD
type: SiteQuality
SIO_000300: 6.88e0

GenotypeQuality
all individuals: 343
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18128
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 914
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variant carriers: 0

GenotypeQuality
all individuals: 474
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GenotypeQuality
all individuals: 138
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variant carriers: 0

GenotypeQuality
all individuals: 4106
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1050
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GenotypeQuality
all individuals: 1415
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 543
bin: 7.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13018
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6364
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7770
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 700
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49878
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5694
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.241002730206007e-4
allele num: 8058
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.011e1

MQRankSum
type: SiteQuality
SIO_000300: 7.87e-1

DP
type: SiteQuality
SIO_000300: 1.036236e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.3786e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: -6.395999999999999e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

QD
type: SiteQuality
SIO_000300: 6.91e0

GenotypeQuality
all individuals: 509
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2422
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 2.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 1417
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 368
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variant carriers: 0

GenotypeQuality
all individuals: 771
bin: 4.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.966800409094485e-5
allele num: 50844
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7968
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6460
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5768
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13178
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.51e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.66e0

VQSLOD
type: SiteQuality
SIO_000300: 4.86e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

DP
type: SiteQuality
SIO_000300: 1.062641e6

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.249e1

GenotypeQuality
all individuals: 86
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variant carriers: 0

GenotypeQuality
all individuals: 2708
bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3176
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1423
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GenotypeQuality
all individuals: 25200
bin: 6.25e1
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GenotypeQuality
all individuals: 187
bin: 9.25e1
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GenotypeQuality
all individuals: 153
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 982
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5962
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13792
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8484
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.863238308179616e-5
allele num: 53670
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8558
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 750
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6778
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.343e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-3

VQSLOD
type: SiteQuality
SIO_000300: -9.304e-1

DP
type: SiteQuality
SIO_000300: 1.131768e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.24e0

FS
type: SiteQuality
SIO_000300: 1.0118e1

MQRankSum
type: SiteQuality
SIO_000300: 2.35e-1

QD
type: SiteQuality
SIO_000300: 1.22e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.17e0

MQ
type: SiteQuality
SIO_000300: 5.929e1

GenotypeQuality
all individuals: 23176
bin: 6.25e1
variant carriers: 8

GenotypeQuality
all individuals: 2592
bin: 6.75e1
variant carriers: 10

GenotypeQuality
all individuals: 682
bin: 7.75e1
variant carriers: 18

GenotypeQuality
all individuals: 191
bin: 9.25e1
variant carriers: 18

GenotypeQuality
all individuals: 1849
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variant carriers: 14

GenotypeQuality
all individuals: 13398
bin: 2.25e1
variant carriers: 6

GenotypeQuality
all individuals: 462
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variant carriers: 5

GenotypeQuality
all individuals: 754
bin: 5.75e1
variant carriers: 8

GenotypeQuality
all individuals: 740
bin: 7.25e1
variant carriers: 13

GenotypeQuality
all individuals: 3026
bin: 2.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3925
bin: 9.75e1
variant carriers: 2590

European (Finnish)
type: Population
allele count: 261
allele frequency: 4.339873628200865e-2
allele num: 6014
num of homozygotes: 6

Other
type: Population
allele count: 33
allele frequency: 4.319371727748691e-2
allele num: 764
num of homozygotes: 1

African
type: Population
allele count: 58
allele frequency: 6.761482863138261e-3
allele num: 8578
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2194
allele frequency: 4.026131317209234e-2
allele num: 54494
num of homozygotes: 43

Latino
type: Population
allele count: 98
allele frequency: 1.141392965292336e-2
allele num: 8586
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6812
num of homozygotes: 0

South Asian
type: Population
allele count: 73
allele frequency: 5.271519352975159e-3
allele num: 13848
num of homozygotes: 1

QD
type: SiteQuality
SIO_000300: 1.495e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.15e-2

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.22e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.177902e6

VQSLOD
type: SiteQuality
SIO_000300: 6.87e0

GenotypeQuality
all individuals: 1132
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1591
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 534
bin: 5.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2497
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 534
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 13522
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 204
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variant carriers: 0

GenotypeQuality
all individuals: 1762
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1823
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2857
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6828
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6030
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 764
num of homozygotes: 0

South Asian
type: Population
allele count: 7
allele frequency: 5.057803468208092e-4
allele num: 13840
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 4.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.429e0

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.04e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.162311e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.7e-1

QD
type: SiteQuality
SIO_000300: 1.042e1

GenotypeQuality
all individuals: 1150
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 201
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 667
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1456
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1589
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2770
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26537
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 898
bin: 7.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7024
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 2.23613595706619e-4
allele num: 8944
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8746
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6118
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14136
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55832
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 774
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.197092e6

VQSLOD
type: SiteQuality
SIO_000300: 3.69e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.35e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.19e-1

FS
type: SiteQuality
SIO_000300: 2.101e0

QD
type: SiteQuality
SIO_000300: 9.83e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.17e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.104e0

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 295
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 923
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27836
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2323
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 895
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 993
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7210
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8872
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14322
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.081314878892734e-4
allele num: 9248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57004
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6176
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.672e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.19e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.92e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.75e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

DP
type: SiteQuality
SIO_000300: 1.225708e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.01e-1

GenotypeQuality
all individuals: 2259
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1623
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1589
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1003
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10888
bin: 2.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9302
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14354
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6178
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.750148762644825e-5
allele num: 57138
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 800
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7230
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8882
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.119e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.58e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

QD
type: SiteQuality
SIO_000300: 1.248e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.884e1

DP
type: SiteQuality
SIO_000300: 1.230244e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.04e0

VQSLOD
type: SiteQuality
SIO_000300: -3.71e-1

GenotypeQuality
all individuals: 3582
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2164
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 613
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 313
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2625
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1058
bin: 7.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 810
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8986
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.726161706828696e-5
allele num: 57932
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7342
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6214
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9520
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.75e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.467e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.105e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

DP
type: SiteQuality
SIO_000300: 1.259582e6

VQSLOD
type: SiteQuality
SIO_000300: -7.366e-1

FS
type: SiteQuality
SIO_000300: 4.545e0

MQ
type: SiteQuality
SIO_000300: 5.895e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.134e1