10-135193957-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135193957
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135193957
    reference: chr 10
allele count: 1
allele frequency: 8.599043786330961e-6
allele num: 116292
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.636C>T
  hgvsp: ENST00000278060.5:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.181+956C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.636C>T
  hgvsp: ENST00000357296.3:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.181+956C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.598C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.636C>T
  hgvsp: ENST00000480071.2:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.181+956C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.636C>T
  hgvsp: ENST00000356306.5:c.636C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.181+956C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1688
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23771
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20153
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8939
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 457
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr212Thr
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: African
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

10-135193964-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135193964
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135193964
    reference: chr 10
allele count: 2
allele frequency: 1.738314182905418e-5
allele num: 115054
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.643C>T
  hgvsp: ENSP00000349847.3:p.Pro215Ser
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.181+963C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.181+963C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.643C>T
  hgvsp: ENSP00000348654.5:p.Pro215Ser
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.643C>T
  hgvsp: ENSP00000435514.1:p.Pro215Ser
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.181+963C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.181+963C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.605C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.643C>T
  hgvsp: ENSP00000278060.5:p.Pro215Ser
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 305
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4736
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1706
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2195
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22519
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 918
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18554
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8710
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 434
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 165
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 44753
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Pro215Ser
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: QD

10-135193965-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135193965
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135193965
    reference: chr 10
allele count: 1
allele frequency: 8.729355075247041e-6
allele num: 114556
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.644C>T
  hgvsp: ENSP00000435514.1:p.Pro215Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.606C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.181+964C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.644C>T
  hgvsp: ENSP00000278060.5:p.Pro215Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.644C>T
  hgvsp: ENSP00000348654.5:p.Pro215Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.644C>T
  hgvsp: ENSP00000349847.3:p.Pro215Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.181+964C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.181+964C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.181+964C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 311
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1097
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2296
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5348
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22091
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1739
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18026
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8701
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 792
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43534
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 408
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Pro215Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD

10-135193966-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135193966
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135193966
    reference: chr 10
allele count: 1
allele frequency: 8.721741557354173e-6
allele num: 114656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.645G>A
  hgvsp: ENST00000480071.2:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.181+965G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.645G>A
  hgvsp: ENST00000278060.5:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.645G>A
  hgvsp: ENST00000356306.5:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.181+965G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.645G>A
  hgvsp: ENST00000357296.3:c.645G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.181+965G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.607G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.181+965G>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1729
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2311
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8646
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5401
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 306
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7106
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro215Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/10-135193975-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135193975
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135193975
    reference: chr 10
allele count: 1
allele frequency: 8.907098957869422e-6
allele num: 112270
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.654C>A
  hgvsp: ENSP00000348654.5:p.Asp218Glu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.654C>A
  hgvsp: ENSP00000435514.1:p.Asp218Glu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.181+974C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.654C>A
  hgvsp: ENSP00000349847.3:p.Asp218Glu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.181+974C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.654C>A
  hgvsp: ENSP00000278060.5:p.Asp218Glu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.181+974C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.181+974C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.616C>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10359
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 913
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14424
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3266
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18628
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7974
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4377
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp218Glu
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

10-135193979-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135193979
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135193979
    reference: chr 10
allele count: 2
allele frequency: 1.818479387536142e-5
allele num: 109982
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.658A>G
  hgvsp: ENSP00000349847.3:p.Thr220Ala
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.181+978A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.658A>G
  hgvsp: ENSP00000435514.1:p.Thr220Ala
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.658A>G
  hgvsp: ENSP00000348654.5:p.Thr220Ala
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.658A>G
  hgvsp: ENSP00000278060.5:p.Thr220Ala
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.181+978A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.620A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.181+978A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.181+978A>G
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15020
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3874
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15471
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1656
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4995
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10468
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7381
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 298
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 182
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 207
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 353
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr220Ala
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

10-135193980-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135193980
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135193980
    reference: chr 10
allele count: 1
allele frequency: 9.051084319901523e-6
allele num: 110484
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.659C>T
  hgvsp: ENSP00000435514.1:p.Thr220Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.659C>T
  hgvsp: ENSP00000348654.5:p.Thr220Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.659C>T
  hgvsp: ENSP00000349847.3:p.Thr220Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.659C>T
  hgvsp: ENSP00000278060.5:p.Thr220Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.181+979C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.621C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.181+979C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.181+979C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.181+979C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15081
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4966
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10382
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1646
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15519
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7360
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2221
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20375
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 123
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Thr220Ile
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS

10-135193993-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135193993
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135193993
    reference: chr 10
allele count: 1
allele frequency: 1.098225267966965e-5
allele num: 91056
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-971C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.668+4C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.668+4C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.668+4C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.668+4C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-971C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.630+4C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-971C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-971C>G
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1743
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1178
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26985
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2381
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3501
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13781
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5147
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7073
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 466
  bin: 2.5e0
  variant carriers: 0
hgvs: c.668+4C>G
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum

10-135193994-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135193994
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135193994
    reference: chr 10
allele count: 3
allele frequency: 3.291855948383698e-5
allele num: 91134
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.668+5G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.668+5G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-970G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.630+5G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-970G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.668+5G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.668+5G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-970G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-970G>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10031
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3539
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 138
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13585
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27073
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2332
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1745
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36450
  bin: 2.25e1
  variant carriers: 0
hgvs: c.668+5G>A
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

10-135193995-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135193995
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135193995
    reference: chr 10
allele count: 10
allele frequency: 1.122737683567611e-4
allele num: 89068
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-969T>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.668+6T>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.630+6T>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-969T>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-969T>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.668+6T>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.668+6T>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.668+6T>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-969T>C
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2270
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10916
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3752
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13347
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26792
  bin: 1.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1633
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 768
  bin: 3.75e1
  variant carriers: 0
hgvs: c.668+6T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ

10-135193996-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135193996
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135193996
    reference: chr 10
allele count: 1
allele frequency: 1.169098391320613e-5
allele num: 85536
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.668+7G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.630+7G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-968G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.668+7G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.668+7G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-968G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.668+7G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-968G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-968G>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26382
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12984
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12037
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2191
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1218
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3929
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3583
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1779
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.25e1
  variant carriers: 0
hgvs: c.668+7G>A
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff

10-135194010-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194010
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194010
    reference: chr 10
allele count: 9
allele frequency: 1.481383941798071e-4
allele num: 60754
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-954C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-954C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.630+21C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-954C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.668+21C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.668+21C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.668+21C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.668+21C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-954C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1184
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6315
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25659
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 4331
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1155
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11325
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32135
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2125
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 255
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: MQ
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/10-135194012-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194012
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194012
    reference: chr 10
allele count: 1
allele frequency: 1.597290994473373e-5
allele num: 62606
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.668+23C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.630+23C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-952C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.668+23C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-952C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.668+23C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-952C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-952C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.668+23C>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25214
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3710
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1456
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 608
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

10-135194012-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194012
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194012
    reference: chr 10
allele count: 1
allele frequency: 1.597290994473373e-5
allele num: 62606
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-952C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.668+23C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.668+23C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-952C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.668+23C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.630+23C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-952C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.668+23C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-952C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25214
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20888
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6347
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3710
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8967
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 705
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

10-135194013-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194013
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194013
    reference: chr 10
allele count: 2090
allele frequency: 3.356890459363958e-2
allele num: 62260
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.630+24G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-951G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.668+24G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-951G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.668+24G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.668+24G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-951G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.668+24G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-951G>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6242
  bin: 2.5e0
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 21244
  bin: 7.5e0
  variant carriers: 463
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 2.75e1
  variant carriers: 84
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 1.75e1
  variant carriers: 705
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 24728
  bin: 1.25e1
  variant carriers: 908
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.25e1
  variant carriers: 30
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 2.25e1
  variant carriers: 300
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2043
  bin: 9.75e1
  variant carriers: 1889
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 8.75e1
  variant carriers: 68
genotype quality: GenotypeQuality
  all individuals: 497
  bin: 3.75e1
  variant carriers: 19
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 7.25e1
  variant carriers: 42
genotype quality: GenotypeQuality
  all individuals: 2647
  bin: 6.25e1
  variant carriers: 35
num of homozygotes: 41
population: Latino
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD

10-135194013-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194013
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194013
    reference: chr 10
allele count: 2
allele frequency: 3.2123353678124e-5
allele num: 62260
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-951G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.668+24G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.630+24G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.668+24G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-951G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-951G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.668+24G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-951G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.668+24G>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21244
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2098
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6242
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3513
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24728
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1165
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3708
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2043
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: Latino
reference allele: G
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

10-135194014-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194014
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194014
    reference: chr 10
allele count: 2
allele frequency: 3.330336030905518e-5
allele num: 60054
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.668+25C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-950C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.668+25C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-950C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-950C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.668+25C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.668+25C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.630+25C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-950C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2831
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22115
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1162
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6914
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24533
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 578
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: African
population: East Asian
population: South Asian
reference allele: C
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum

10-135194037-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194037
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194037
    reference: chr 10
allele count: 1
allele frequency: 2.353384166431328e-5
allele num: 42492
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.668+48A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-927A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.630+48A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-927A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-927A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-927A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.668+48A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.668+48A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.668+48A>G
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3246
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 787
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28353
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9094
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 495
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22422
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: QD

10-135194916-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194916
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194916
    reference: chr 10
allele count: 24
allele frequency: 2.08568697314678e-4
allele num: 115070
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-48C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-48C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-48C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-48C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-48C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-48C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-48C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-48C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-48C>G
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2547
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10100
  bin: 2.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16700
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 13458
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9564
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1615
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4685
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 723
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4943
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5917
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5614
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2974
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

10-135194920-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194920
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194920
    reference: chr 10
allele count: 3
allele frequency: 2.60321757692508e-5
allele num: 115242
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-44C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-44C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-44C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-44C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-44C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-44C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-44C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-44C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-44C>G
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9265
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2536
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9403
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4800
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20524
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1654
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4730
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1984
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

10-135194924-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194924
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194924
    reference: chr 10
allele count: 1
allele frequency: 8.653663095588363e-6
allele num: 115558
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-40G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-40G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-40G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-40G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-40G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-40G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-40G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-40G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-40G>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11221
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8379
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5016
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6265
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2485
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23729
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 282
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1637
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2004
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1212
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6363
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3011
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1827
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD

10-135194925-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194925
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194925
    reference: chr 10
allele count: 1
allele frequency: 8.648873051841344e-6
allele num: 115622
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-39G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-39G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-39G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-39G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-39G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-39G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-39G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-39G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-39G>C
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5045
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5794
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11375
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 278
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1640
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24236
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1422
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 464
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

10-135194926-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194926
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194926
    reference: chr 10
allele count: 10
allele frequency: 8.639159582555809e-5
allele num: 115752
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-38A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-38A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-38A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-38A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-38A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-38A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-38A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-38A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-38A>G
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7948
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24824
  bin: 2.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5289
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11505
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1643
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1431
  bin: 9.75e1
  variant carriers: 10
genotype quality: GenotypeQuality
  all individuals: 2954
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 217
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28744
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: Other
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff

10-135194932-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194932
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194932
    reference: chr 10
allele count: 2
allele frequency: 1.722801274872944e-5
allele num: 116090
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-32C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-32C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-32C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-32C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-32C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-32C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-32C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-32C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-32C>G
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1668
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 224
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2272
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27472
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12639
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3159
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5475
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6093
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1489
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2667
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

10-135194933-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194933
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194933
    reference: chr 10
allele count: 1
allele frequency: 8.600079120727911e-6
allele num: 116278
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-31C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-31C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-31C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-31C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-31C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-31C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-31C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-31C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-31C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5700
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5526
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27924
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12867
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2856
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1676
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 619
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2322
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1428
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

10-135194935-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194935
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194935
    reference: chr 10
allele count: 1
allele frequency: 8.581775741036335e-6
allele num: 116526
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-29C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-29C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-29C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-29C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-29C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-29C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-29C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-29C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-29C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4936
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13161
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2145
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29095
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 548
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 348
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7076
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1306
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

10-135194938-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194938
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194938
    reference: chr 10
allele count: 663
allele frequency: 5.67209636575183e-3
allele num: 116888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-26C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-26C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-26C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-26C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-26C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-26C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-26C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-26C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-26C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1735
  bin: 3.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 3805
  bin: 1.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5797
  bin: 3.25e1
  variant carriers: 81
genotype depth: GenotypeDepth
  all individuals: 13652
  bin: 2.75e1
  variant carriers: 90
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1521
  bin: 1.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 5.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.25e1
  variant carriers: 53
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 9.75e1
  variant carriers: 43
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 383
  bin: 4.75e1
  variant carriers: 51
genotype depth: GenotypeDepth
  all individuals: 30230
  bin: 2.25e1
  variant carriers: 99
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 6.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1736
  bin: 3.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 8.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 5.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2248
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 14
population: European (Finnish)
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: C
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

10-135194939-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194939
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194939
    reference: chr 10
allele count: 5
allele frequency: 4.266648462299894e-5
allele num: 117188
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-25G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-25G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-25G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-25G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-25G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-25G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-25G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-25G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-25G>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13985
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30778
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37191
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 298
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
population: Other
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD

10-135194939-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194939
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194939
    reference: chr 10
allele count: 1
allele frequency: 8.533296924599789e-6
allele num: 117188
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-25G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-25G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-25G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-25G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-25G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-25G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-25G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-25G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-25G>C
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30778
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1255
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1849
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13985
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1753
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37191
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1098
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS

10-135194942-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194942
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194942
    reference: chr 10
allele count: 1
allele frequency: 8.491703605577351e-6
allele num: 117762
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-22A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-22A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-22A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-22A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-22A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-22A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-22A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-22A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-22A>G
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32047
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5962
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2452
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38809
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 520
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1395
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 715
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

10-135194942-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194942
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194942
    reference: chr 10
allele count: 12
allele frequency: 1.019004432669282e-4
allele num: 117762
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-22A>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-22A>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-22A>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-22A>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-22A>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-22A>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-22A>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-22A>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-22A>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14192
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5962
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32047
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2480
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 749
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1624
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1754
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1859
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 147
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 302
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

10-135194946-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194946
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194946
    reference: chr 10
allele count: 1
allele frequency: 8.460523198754612e-6
allele num: 118196
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-18G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-18G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-18G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-18G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-18G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-18G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-18G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-18G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-18G>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1764
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1848
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 609
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32406
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14681
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6164
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 232
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 215
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1412
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

10-135194951-TC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194951
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194950
    reference: chr 10
allele count: 1
allele frequency: 8.419351036422112e-6
allele num: 118774
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-11delC
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-11delC
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-11delC
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-11delC
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-11delC
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-11delC
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-11delC
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-11delC
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-11delC
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 757
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1143
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1767
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1241
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15097
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40296
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1450
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 533
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: TC
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum

10-135194952-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194952
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194952
    reference: chr 10
allele count: 2
allele frequency: 1.682651859330305e-5
allele num: 118860
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-12C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-12C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-12C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-12C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-12C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-12C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-12C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-12C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-12C>G
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6337
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1770
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 760
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32994
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2447
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7915
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 667
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP

10-135194953-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194953
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194953
    reference: chr 10
allele count: 17
allele frequency: 1.429460336679952e-4
allele num: 118926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-11C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-11C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-11C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-11C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-11C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-11C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-11C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-11C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-11C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6398
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32951
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1786
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 15290
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 766
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2558
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ

10-135194954-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194954
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194954
    reference: chr 10
allele count: 113
allele frequency: 9.490694080494524e-4
allele num: 119064
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-10G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-10G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-10G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-10G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-10G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-10G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-10G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-10G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-10G>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32949
  bin: 2.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15375
  bin: 2.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 3.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 3.25e1
  variant carriers: 12
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1115
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

10-135194954-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194954
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194954
    reference: chr 10
allele count: 1
allele frequency: 8.398844319021702e-6
allele num: 119064
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-10G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-10G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-10G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-10G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-10G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-10G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-10G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-10G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-10G>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 193
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15375
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1787
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6434
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7966
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/10-135194960-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194960
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194960
    reference: chr 10
allele count: 1
allele frequency: 8.368060785593547e-6
allele num: 119502
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.669-4C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.182-4C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.669-4C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.669-4C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.669-4C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.631-4C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.182-4C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.182-4C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.182-4C>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 645
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 810
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6524
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15644
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1807
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 218
  bin: 2.75e1
  variant carriers: 0
hgvs: c.669-4C>A
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

10-135194974-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194974
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194974
    reference: chr 10
allele count: 1
allele frequency: 8.325562808045825e-6
allele num: 120112
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.192G>C
  hgvsp: ENSP00000434550.1:p.Lys64Asn
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.679G>C
  hgvsp: ENSP00000278060.5:p.Gly227Arg
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.192G>C
  hgvsp: ENSP00000432737.1:p.Lys64Asn
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.192G>C
  hgvsp: ENSP00000432517.1:p.Lys64Asn
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.679G>C
  hgvsp: ENSP00000348654.5:p.Gly227Arg
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.641G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.192G>C
  hgvsp: ENSP00000357527.4:p.Lys64Asn
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.679G>C
  hgvsp: ENSP00000349847.3:p.Gly227Arg
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.679G>C
  hgvsp: ENSP00000435514.1:p.Gly227Arg
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33181
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1831
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6760
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16188
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8243
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 681
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly227Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: QD

10-135194981-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194981
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194981
    reference: chr 10
allele count: 1
allele frequency: 8.314763694415805e-6
allele num: 120268
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.648C>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.199C>G
  hgvsp: ENSP00000432517.1:p.Gln67Glu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.199C>G
  hgvsp: ENSP00000434550.1:p.Gln67Glu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.686C>G
  hgvsp: ENSP00000349847.3:p.Thr229Arg
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.686C>G
  hgvsp: ENSP00000278060.5:p.Thr229Arg
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.199C>G
  hgvsp: ENSP00000357527.4:p.Gln67Glu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.686C>G
  hgvsp: ENSP00000348654.5:p.Thr229Arg
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.199C>G
  hgvsp: ENSP00000432737.1:p.Gln67Glu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.686C>G
  hgvsp: ENSP00000435514.1:p.Thr229Arg
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6799
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Thr229Arg
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ

10-135194981-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194981
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194981
    reference: chr 10
allele count: 1
allele frequency: 8.314763694415805e-6
allele num: 120268
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.686C>T
  hgvsp: ENSP00000348654.5:p.Thr229Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.199C>T
  hgvsp: ENSP00000432517.1:p.Gln67Ter
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.686C>T
  hgvsp: ENSP00000435514.1:p.Thr229Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.199C>T
  hgvsp: ENSP00000432737.1:p.Gln67Ter
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.648C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.199C>T
  hgvsp: ENSP00000434550.1:p.Gln67Ter
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.199C>T
  hgvsp: ENSP00000357527.4:p.Gln67Ter
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.686C>T
  hgvsp: ENSP00000349847.3:p.Thr229Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.686C>T
  hgvsp: ENSP00000278060.5:p.Thr229Ile
  variant of: http://identifiers.org/hgnc/20837
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1836
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16338
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6799
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33140
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8297
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2589
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Gln67Ter
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: Latino
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: MQRankSum

10-135194987-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194987
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194987
    reference: chr 10
allele count: 1
allele frequency: 8.312690152787244e-6
allele num: 120298
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.692G>C
  hgvsp: ENSP00000348654.5:p.Cys231Ser
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.205G>C
  hgvsp: ENSP00000434550.1:p.Ala69Pro
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.692G>C
  hgvsp: ENSP00000349847.3:p.Cys231Ser
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.205G>C
  hgvsp: ENSP00000432737.1:p.Ala69Pro
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.692G>C
  hgvsp: ENSP00000278060.5:p.Cys231Ser
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.205G>C
  hgvsp: ENSP00000432517.1:p.Ala69Pro
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.205G>C
  hgvsp: ENSP00000357527.4:p.Ala69Pro
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.654G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.692G>C
  hgvsp: ENSP00000435514.1:p.Cys231Ser
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 443
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1838
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16420
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6815
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 480
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8321
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Cys231Ser
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD

10-135194988-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194988
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194988
    reference: chr 10
allele count: 1
allele frequency: 8.311722853913159e-6
allele num: 120312
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.206C>T
  hgvsp: ENSP00000357527.4:p.Ala69Val
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.655C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.693C>T
  hgvsp: ENST00000278060.5:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.693C>T
  hgvsp: ENST00000480071.2:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.206C>T
  hgvsp: ENSP00000434550.1:p.Ala69Val
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.693C>T
  hgvsp: ENST00000357296.3:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.206C>T
  hgvsp: ENSP00000432737.1:p.Ala69Val
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.206C>T
  hgvsp: ENSP00000432517.1:p.Ala69Val
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.693C>T
  hgvsp: ENST00000356306.5:c.693C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 222
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16440
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33041
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 438
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41886
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala69Val
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ

10-135194989-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194989
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194989
    reference: chr 10
allele count: 2
allele frequency: 1.662344570782632e-5
allele num: 120312
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.656A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.207A>G
  hgvsp: ENST00000483211.2:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.694A>G
  hgvsp: ENSP00000278060.5:p.Met232Val
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.207A>G
  hgvsp: ENST00000476834.2:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.694A>G
  hgvsp: ENSP00000349847.3:p.Met232Val
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.694A>G
  hgvsp: ENSP00000348654.5:p.Met232Val
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.694A>G
  hgvsp: ENSP00000435514.1:p.Met232Val
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.207A>G
  hgvsp: ENST00000529585.1:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.207A>G
  hgvsp: ENST00000368539.4:c.207A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16468
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6822
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1841
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 472
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2674
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Met232Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: A
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

10-135194998-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135194998
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135194998
    reference: chr 10
allele count: 1
allele frequency: 8.307027745472669e-6
allele num: 120380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.703G>A
  hgvsp: ENSP00000435514.1:p.Ala235Thr
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*6G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.703G>A
  hgvsp: ENSP00000348654.5:p.Ala235Thr
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.703G>A
  hgvsp: ENSP00000349847.3:p.Ala235Thr
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*6G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*6G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.703G>A
  hgvsp: ENSP00000278060.5:p.Ala235Thr
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.665G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*6G>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1859
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16610
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 785
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2592
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41877
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala235Thr
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/10-135195000-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195000
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195000
    reference: chr 10
allele count: 1
allele frequency: 8.304682179812978e-6
allele num: 120414
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*8C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.667C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*8C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.705C>A
  hgvsp: ENST00000356306.5:c.705C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.705C>A
  hgvsp: ENST00000278060.5:c.705C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.705C>A
  hgvsp: ENST00000357296.3:c.705C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.705C>A
  hgvsp: ENST00000480071.2:c.705C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*8C>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*8C>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 423
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1530
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala235Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: Other
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum

10-135195000-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195000
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195000
    reference: chr 10
allele count: 1
allele frequency: 8.304682179812978e-6
allele num: 120414
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.667C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.705C>T
  hgvsp: ENST00000278060.5:c.705C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*8C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.705C>T
  hgvsp: ENST00000356306.5:c.705C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*8C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.705C>T
  hgvsp: ENST00000357296.3:c.705C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.705C>T
  hgvsp: ENST00000480071.2:c.705C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*8C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*8C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 32828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 186
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16649
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 687
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala235Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

10-135195005-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195005
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195005
    reference: chr 10
allele count: 126
allele frequency: 1.046198810986748e-3
allele num: 120436
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.710C>T
  hgvsp: ENSP00000349847.3:p.Pro237Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.710C>T
  hgvsp: ENSP00000348654.5:p.Pro237Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.710C>T
  hgvsp: ENSP00000435514.1:p.Pro237Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*13C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*13C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*13C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.710C>T
  hgvsp: ENSP00000278060.5:p.Pro237Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.672C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*13C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 197
  bin: 5.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32630
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6911
  bin: 3.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 3.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 8.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 16690
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.25e1
  variant carriers: 6
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1518
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro237Leu
num of homozygotes: 1
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum

10-135195006-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195006
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195006
    reference: chr 10
allele count: 5
allele frequency: 4.151789421240555e-5
allele num: 120430
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.711G>A
  hgvsp: ENST00000357296.3:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*14G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.711G>A
  hgvsp: ENST00000356306.5:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.711G>A
  hgvsp: ENST00000480071.2:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.673G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.711G>A
  hgvsp: ENST00000278060.5:c.711G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*14G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*14G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*14G>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16691
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 374
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6934
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32591
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1516
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8339
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Pro237Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: MQ

10-135195009-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195009
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195009
    reference: chr 10
allele count: 1
allele frequency: 8.303027283747654e-6
allele num: 120438
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*17G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.714G>A
  hgvsp: ENST00000480071.2:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.714G>A
  hgvsp: ENST00000357296.3:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.676G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*17G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*17G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.714G>A
  hgvsp: ENST00000278060.5:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*17G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.714G>A
  hgvsp: ENST00000356306.5:c.714G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 373
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32575
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16722
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6928
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Glu238Glu
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP

10-135195010-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195010
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195010
    reference: chr 10
allele count: 1
allele frequency: 8.301786544464368e-6
allele num: 120456
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*18G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.715G>A
  hgvsp: ENSP00000348654.5:p.Asp239Asn
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.677G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.715G>A
  hgvsp: ENSP00000349847.3:p.Asp239Asn
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.715G>A
  hgvsp: ENSP00000435514.1:p.Asp239Asn
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.715G>A
  hgvsp: ENSP00000278060.5:p.Asp239Asn
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*18G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*18G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*18G>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 790
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1877
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16740
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 369
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6926
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32567
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41893
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 550
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp239Asn
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: Other
population: European (Finnish)
population: African
reference allele: G
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum

http://identifiers.org/exac.variant/10-135195011-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195011
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195011
    reference: chr 10
allele count: 1
allele frequency: 8.301648707433296e-6
allele num: 120458
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*19A>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.716A>C
  hgvsp: ENSP00000349847.3:p.Asp239Ala
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*19A>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*19A>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*19A>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.678A>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.716A>C
  hgvsp: ENSP00000278060.5:p.Asp239Ala
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.716A>C
  hgvsp: ENSP00000435514.1:p.Asp239Ala
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.716A>C
  hgvsp: ENSP00000348654.5:p.Asp239Ala
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16735
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6920
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 789
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1514
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asp239Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ

10-135195014-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195014
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195014
    reference: chr 10
allele count: 1
allele frequency: 8.299995020002988e-6
allele num: 120482
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.719C>T
  hgvsp: ENSP00000349847.3:p.Thr240Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.681C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.719C>T
  hgvsp: ENSP00000435514.1:p.Thr240Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*22C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*22C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.719C>T
  hgvsp: ENSP00000348654.5:p.Thr240Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.719C>T
  hgvsp: ENSP00000278060.5:p.Thr240Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*22C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*22C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 693
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41865
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr240Ile
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ClippingRankSum

10-135195014-CTG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195014
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195012
    reference: chr 10
allele count: 1
allele frequency: 8.299995020002988e-6
allele num: 120482
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*24_*25delGT
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.721_722delGT
  hgvsp: ENSP00000348654.5:p.Val241SerfsTer3
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.721_722delGT
  hgvsp: ENSP00000435514.1:p.Val241SerfsTer3
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.683_684delGT
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.721_722delGT
  hgvsp: ENSP00000278060.5:p.Val241SerfsTer3
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.721_722delGT
  hgvsp: ENSP00000349847.3:p.Val241SerfsTer3
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*24_*25delGT
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*24_*25delGT
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*24_*25delGT
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32548
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6923
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1881
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 791
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 175
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2673
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val241SerfsTer3
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Latino
reference allele: CTG
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP

10-135195016-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195016
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195016
    reference: chr 10
allele count: 0
allele frequency: 0.0e0
allele num: 120458
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.721G>A
  hgvsp: ENSP00000278060.5:p.Val241Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.721G>A
  hgvsp: ENSP00000349847.3:p.Val241Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*24G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*24G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.721G>A
  hgvsp: ENSP00000435514.1:p.Val241Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*24G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.721G>A
  hgvsp: ENSP00000348654.5:p.Val241Ile
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*24G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.683G>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1879
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16753
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 795
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32531
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 372
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6930
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8363
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Val241Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/10-135195018-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195018
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195018
    reference: chr 10
allele count: 2
allele frequency: 1.66008167601846e-5
allele num: 120476
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.723A>C
  hgvsp: ENST00000356306.5:c.723A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.723A>C
  hgvsp: ENST00000278060.5:c.723A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*26A>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.723A>C
  hgvsp: ENST00000480071.2:c.723A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.723A>C
  hgvsp: ENST00000357296.3:c.723A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*26A>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*26A>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.685A>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*26A>C
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Val241Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

10-135195018-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195018
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195018
    reference: chr 10
allele count: 2
allele frequency: 1.66008167601846e-5
allele num: 120476
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*26A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*26A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.723A>G
  hgvsp: ENST00000357296.3:c.723A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.723A>G
  hgvsp: ENST00000356306.5:c.723A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.723A>G
  hgvsp: ENST00000480071.2:c.723A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*26A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.723A>G
  hgvsp: ENST00000278060.5:c.723A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*26A>G
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.685A>G
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32525
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 370
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 205
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 801
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1876
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6933
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16751
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1478
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Val241Val
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum

10-135195032-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195032
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195032
    reference: chr 10
allele count: 2
allele frequency: 1.659090154959021e-5
allele num: 120548
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*40C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.737C>T
  hgvsp: ENSP00000278060.5:p.Pro246Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.737C>T
  hgvsp: ENSP00000435514.1:p.Pro246Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*40C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.737C>T
  hgvsp: ENSP00000349847.3:p.Pro246Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.699C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.737C>T
  hgvsp: ENSP00000348654.5:p.Pro246Leu
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*40C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*40C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7004
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16894
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 805
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1897
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 82
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro246Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
reference allele: C
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum

10-135195033-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195033
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195033
    reference: chr 10
allele count: 3
allele frequency: 2.488470088589535e-5
allele num: 120556
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.738T>C
  hgvsp: ENST00000357296.3:c.738T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*41T>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.700T>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*41T>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*41T>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.738T>C
  hgvsp: ENST00000356306.5:c.738T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.738T>C
  hgvsp: ENST00000480071.2:c.738T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*41T>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.738T>C
  hgvsp: ENST00000278060.5:c.738T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 210
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16897
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32305
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7014
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1898
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41781
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 551
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2669
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 699
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Pro246Pro
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

http://identifiers.org/exac.variant/10-135195040-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195040
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195040
    reference: chr 10
allele count: 16
allele frequency: 1.333022294797881e-4
allele num: 120028
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.745A>C
  hgvsp: ENSP00000435514.1:p.Thr249Pro
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.707A>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*48A>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.745A>C
  hgvsp: ENSP00000349847.3:p.Thr249Pro
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*48A>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.745A>C
  hgvsp: ENSP00000348654.5:p.Thr249Pro
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*48A>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.745A>C
  hgvsp: ENSP00000278060.5:p.Thr249Pro
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*48A>C
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.90to99.95
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16827
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1979
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7064
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 859
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 32078
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 41348
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.75e1
  variant carriers: 1
hgvs: p.Thr249Pro
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: A
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: DP

10-135195042-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195042
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195042
    reference: chr 10
allele count: 1
allele frequency: 8.292561572269675e-6
allele num: 120590
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*50C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.747C>T
  hgvsp: ENST00000278060.5:c.747C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*50C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.747C>T
  hgvsp: ENST00000357296.3:c.747C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*50C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*50C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.709C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.747C>T
  hgvsp: ENST00000356306.5:c.747C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.747C>T
  hgvsp: ENST00000480071.2:c.747C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7196
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1919
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32075
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17152
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 380
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr249Thr
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

10-135195050-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195050
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195050
    reference: chr 10
allele count: 1
allele frequency: 8.290774026663129e-6
allele num: 120616
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*58G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.755G>A
  hgvsp: ENSP00000435514.1:p.Trp252Ter
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*58G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*58G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.755G>A
  hgvsp: ENSP00000349847.3:p.Trp252Ter
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*58G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.755G>A
  hgvsp: ENSP00000278060.5:p.Trp252Ter
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.717G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.755G>A
  hgvsp: ENSP00000348654.5:p.Trp252Ter
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 779
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 189
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7192
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32058
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17211
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2658
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2599
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8434
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Trp252Ter
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

10-135195051-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195051
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195051
    reference: chr 10
allele count: 1
allele frequency: 8.290911502810618e-6
allele num: 120614
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*59G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*59G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.756G>C
  hgvsp: ENSP00000349847.3:p.Trp252Cys
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*59G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*59G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.756G>C
  hgvsp: ENSP00000435514.1:p.Trp252Cys
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.718G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.756G>C
  hgvsp: ENSP00000278060.5:p.Trp252Cys
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.756G>C
  hgvsp: ENSP00000348654.5:p.Trp252Cys
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17210
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7198
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 147
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 357
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 775
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Trp252Cys
num of homozygotes: 0
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum

10-135195054-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195054
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195054
    reference: chr 10
allele count: 11
allele frequency: 9.120305115662051e-5
allele num: 120610
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*62C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.759C>T
  hgvsp: ENST00000356306.5:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*62C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.759C>T
  hgvsp: ENST00000278060.5:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.759C>T
  hgvsp: ENST00000480071.2:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*62C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.759C>T
  hgvsp: ENST00000357296.3:c.759C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*62C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.721C>T
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1923
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7214
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 9.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 17207
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 543
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 683
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2597
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asn253Asn
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

10-135195055-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195055
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195055
    reference: chr 10
allele count: 3
allele frequency: 2.487355940635105e-5
allele num: 120610
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.760G>T
  hgvsp: ENSP00000348654.5:p.Gly254Trp
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.760G>T
  hgvsp: ENSP00000349847.3:p.Gly254Trp
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.722G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*63G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.760G>T
  hgvsp: ENSP00000278060.5:p.Gly254Trp
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*63G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*63G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*63G>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.760G>T
  hgvsp: ENSP00000435514.1:p.Gly254Trp
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 192
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17221
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7219
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32012
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 368
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2660
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Gly254Trp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

10-135195057-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195057
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195057
    reference: chr 10
allele count: 2
allele frequency: 1.658182300562124e-5
allele num: 120614
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.724G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.762G>A
  hgvsp: ENST00000356306.5:c.762G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*65G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*65G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.762G>A
  hgvsp: ENST00000357296.3:c.762G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.762G>A
  hgvsp: ENST00000278060.5:c.762G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*65G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.762G>A
  hgvsp: ENST00000480071.2:c.762G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*65G>A
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32015
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7212
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly254Gly
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

10-135195066-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195066
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195066
    reference: chr 10
allele count: 1
allele frequency: 8.290361625574107e-6
allele num: 120622
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.771G>C
  hgvsp: ENSP00000348654.5:p.Gln257His
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.771G>C
  hgvsp: ENSP00000349847.3:p.Gln257His
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.733G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*74G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.771G>C
  hgvsp: ENSP00000435514.1:p.Gln257His
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*74G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*74G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*74G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.771G>C
  hgvsp: ENSP00000278060.5:p.Gln257His
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17287
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32023
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2596
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1405
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Gln257His
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum

10-135195073-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195073
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195073
    reference: chr 10
allele count: 3
allele frequency: 2.486861083939851e-5
allele num: 120634
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*81G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.778G>A
  hgvsp: ENSP00000435514.1:p.Ala260Thr
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.740G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*81G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.778G>A
  hgvsp: ENSP00000349847.3:p.Ala260Thr
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*81G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.778G>A
  hgvsp: ENSP00000278060.5:p.Ala260Thr
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*81G>A
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.778G>A
  hgvsp: ENSP00000348654.5:p.Ala260Thr
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7218
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8455
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala260Thr
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: G
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

10-135195073-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195073
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195073
    reference: chr 10
allele count: 1
allele frequency: 8.28953694646617e-6
allele num: 120634
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*81G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*81G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.778G>C
  hgvsp: ENSP00000348654.5:p.Ala260Pro
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*81G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*81G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.740G>C
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.778G>C
  hgvsp: ENSP00000435514.1:p.Ala260Pro
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.778G>C
  hgvsp: ENSP00000278060.5:p.Ala260Pro
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.778G>C
  hgvsp: ENSP00000349847.3:p.Ala260Pro
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17311
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1921
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31995
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42218
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 350
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala260Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

10-135195079-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 135195079
    reference: chr 10
  end: Position
    type: ExactPosition
    position: 135195079
    reference: chr 10
allele count: 1
allele frequency: 8.290774026663129e-6
allele num: 120616
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432737
  ensembl transcript: ENST00000476834
  gene symbol: PAOX
  hgvsc: ENST00000476834.2:c.*87C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000432517
  ensembl transcript: ENST00000529585
  gene symbol: PAOX
  hgvsc: ENST00000529585.1:c.*87C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000357527
  ensembl transcript: ENST00000368539
  gene symbol: PAOX
  hgvsc: ENST00000368539.4:c.*87C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000349847
  ensembl transcript: ENST00000357296
  gene symbol: PAOX
  hgvsc: ENST00000357296.3:c.784C>T
  hgvsp: ENSP00000349847.3:p.Pro262Ser
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000348654
  ensembl transcript: ENST00000356306
  gene symbol: PAOX
  hgvsc: ENST00000356306.5:c.784C>T
  hgvsp: ENSP00000348654.5:p.Pro262Ser
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000435514
  ensembl transcript: ENST00000480071
  gene symbol: PAOX
  hgvsc: ENST00000480071.2:c.784C>T
  hgvsp: ENSP00000435514.1:p.Pro262Ser
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000434550
  ensembl transcript: ENST00000483211
  gene symbol: PAOX
  hgvsc: ENST00000483211.2:c.*87C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000148832
  ensembl transcript: ENST00000368535
  gene symbol: PAOX
  hgvsc: ENST00000368535.2:n.746C>T
  variant of: http://identifiers.org/hgnc/20837
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000148832
  ensembl protein: ENSP00000278060
  ensembl transcript: ENST00000278060
  gene symbol: PAOX
  hgvsc: ENST00000278060.5:c.784C>T
  hgvsp: ENSP00000278060.5:p.Pro262Ser
  variant of: http://identifiers.org/hgnc/20837
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17333
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31988
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1922
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7209
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Pro262Ser
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 47416
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 48
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3744
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 400
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 688
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 721
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5617
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 3.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63918
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.162188809465122e-5
allele num: 16228
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6118
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 844
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9344
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.72e-1

QD
type: SiteQuality
SIO_000300: 1.0e1

FS
type: SiteQuality
SIO_000300: 2.131e0

DP
type: SiteQuality
SIO_000300: 1.510245e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.51e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.115e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

GenotypeQuality
all individuals: 413
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 219
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6289
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 203
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 760
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 641
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 9.25e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9238
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.158160687215766e-5
allele num: 63328
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8388
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11300
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15958
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.63e-1

MQ
type: SiteQuality
SIO_000300: 5.932e1

MQRankSum
type: SiteQuality
SIO_000300: 1.63e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.6e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.419e0

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

FS
type: SiteQuality
SIO_000300: 2.357e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.36e-1

DP
type: SiteQuality
SIO_000300: 1.468293e6

QD
type: SiteQuality
SIO_000300: 1.201e1

GenotypeQuality
all individuals: 713
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 470
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6966
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 278
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 615
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 84
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 111
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4980
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5826
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.194172438500119e-4
allele num: 8374
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15896
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9196
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63152
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.2e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

QD
type: SiteQuality
SIO_000300: 1.204e1

FS
type: SiteQuality
SIO_000300: 1.084e0

MQRankSum
type: SiteQuality
SIO_000300: 4.57e-1

DP
type: SiteQuality
SIO_000300: 1.457591e6

MQ
type: SiteQuality
SIO_000300: 5.944e1

VQSLOD
type: SiteQuality
SIO_000300: 9.2e-1

GenotypeQuality
all individuals: 122
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44060
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 251
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 130
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4953
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 54
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 602
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 8.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15892
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11278
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.195028680688336e-4
allele num: 8368
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9202
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 834
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5954
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.456244e6

QD
type: SiteQuality
SIO_000300: 1.175e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

MQRankSum
type: SiteQuality
SIO_000300: -1.052e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.49e-1

FS
type: SiteQuality
SIO_000300: 4.316e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.21e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.88e-1

GenotypeQuality
all individuals: 89
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13647
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1408
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 515
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 36897
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 199
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 8.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 820
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11078
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62110
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8260
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.515506906437321e-5
allele num: 15348
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8978
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5676
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.46e-1

DP
type: SiteQuality
SIO_000300: 1.353602e6

QD
type: SiteQuality
SIO_000300: 9.82e0

FS
type: SiteQuality
SIO_000300: 2.682e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQRankSum
type: SiteQuality
SIO_000300: 2.08e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.27e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.379e0

GenotypeQuality
all individuals: 28797
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1198
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1262
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 287
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2184
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 631
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 246
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 20035
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3614
bin: 6.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14974
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8768
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8150
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5312
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10914
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.275359470701909e-5
allele num: 61062
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 802
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.23e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.49e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.45e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.65e-1

DP
type: SiteQuality
SIO_000300: 1.253485e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.5e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.49e-1

QD
type: SiteQuality
SIO_000300: 8.300000000000001e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

GenotypeQuality
all individuals: 111
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 383
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 139
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3628
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 81
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1212
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29458
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1239
bin: 7.5e0
variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 5578
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8158
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.633986928104575e-5
allele num: 61200
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8800
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.252352e6

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -1.878e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.06e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.088e0

MQ
type: SiteQuality
SIO_000300: 5.909e1

VQSLOD
type: SiteQuality
SIO_000300: -2.846e0

FS
type: SiteQuality
SIO_000300: 1.298e0

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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7250
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 51272
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 668
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9172
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4166
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 8.610297916307904e-5
allele num: 11614
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6914
num of homozygotes: 0

QD
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
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DP
type: SiteQuality
SIO_000300: 7.96865e5

FS
type: SiteQuality
SIO_000300: 1.142e0

MQRankSum
type: SiteQuality
SIO_000300: -6.27e-1

BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.51e-2

VQSLOD
type: SiteQuality
SIO_000300: -5.887e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.56e-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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bin: 9.75e1
variant carriers: 3

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9152
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.895142756982043e-5
allele num: 51346
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 7236
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.445504481063891e-4
allele num: 6918
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11626
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 664
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.2121e1

MQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

DP
type: SiteQuality
SIO_000300: 7.93709e5

ClippingRankSum
type: SiteQuality
SIO_000300: 9.13e-1

QD
type: SiteQuality
SIO_000300: 6.59e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.53e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.13e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -2.775e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.357e0

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: 10

GenotypeQuality
all individuals: 115
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 50244
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4062
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6752
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7086
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8966
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 7.958967102935974e-4
allele num: 11308
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.538461538461538e-3
allele num: 650
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 7.75418e5

VQSLOD
type: SiteQuality
SIO_000300: 5.18e-1

FS
type: SiteQuality
SIO_000300: 5.186e0

QD
type: SiteQuality
SIO_000300: 1.021e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.308e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.64e-2

MQRankSum
type: SiteQuality
SIO_000300: -1.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.96e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

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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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6812
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6470
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.067995698568947e-5
allele num: 48356
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10838
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3818
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.856e0

FS
type: SiteQuality
SIO_000300: 7.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

MQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -1.677e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.900000000000001e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.0e0

DP
type: SiteQuality
SIO_000300: 7.55806e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.79e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 2
allele frequency: 2.513194269917064e-4
allele num: 7958
num of homozygotes: 0

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

East Asian
type: Population
allele count: 6
allele frequency: 1.35074290859973e-3
allele num: 4442
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 464
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4692
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 2.878194796223808e-5
allele num: 34744
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6022
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 1.67e0

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 5.33e-1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -7.27e-1

VQSLOD
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SIO_000300: 1.12e0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 482
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele count: 0
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East Asian
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allele frequency: 2.219263204616067e-4
allele num: 4506
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8024
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MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
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FS
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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BaseQRankSum
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VQSLOD
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DP
type: SiteQuality
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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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South Asian
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allele num: 8024
num of homozygotes: 0

East Asian
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allele count: 0
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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African
type: Population
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Other
type: Population
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European (Non-Finnish)
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allele count: 1
allele frequency: 2.769315978953199e-5
allele num: 36110
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Latino
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QD
type: SiteQuality
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MQRankSum
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MQ
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DP
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ReadPosRankSum
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FS
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 350
bin: 6.75e1
variant carriers: 37

Latino
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allele count: 120
allele frequency: 2.004677581022386e-2
allele num: 5986
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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African
type: Population
allele count: 111
allele frequency: 2.288659793814433e-2
allele num: 4850
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European (Non-Finnish)
type: Population
allele count: 1332
allele frequency: 3.710719857365723e-2
allele num: 35896
num of homozygotes: 28

Other
type: Population
allele count: 18
allele frequency: 3.781512605042017e-2
allele num: 476
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European (Finnish)
type: Population
allele count: 166
allele frequency: 6.629392971246006e-2
allele num: 2504
num of homozygotes: 2

South Asian
type: Population
allele count: 343
allele frequency: 4.270418326693227e-2
allele num: 8032
num of homozygotes: 9

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.84e-2

FS
type: SiteQuality
SIO_000300: 6.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

DP
type: SiteQuality
SIO_000300: 6.35636e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.169e0

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.422e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

QD
type: SiteQuality
SIO_000300: 1.312e1

GenotypeQuality
all individuals: 859
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35965
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 135
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1060
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2647
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2375
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8245
bin: 7.5e0
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8032
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 5.571651437486071e-5
allele num: 35896
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4850
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2504
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5986
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.312e1

FS
type: SiteQuality
SIO_000300: 6.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.422e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.84e-2

DP
type: SiteQuality
SIO_000300: 6.35636e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.169e0

MQRankSum
type: SiteQuality
SIO_000300: 2.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.37e0

GenotypeQuality
all individuals: 31
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 36587
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 81
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1399
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2206
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 655
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8870
bin: 7.5e0
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GenotypeQuality
all individuals: 325
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 167
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 205
bin: 5.75e1
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GenotypeQuality
all individuals: 1579
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3996
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2730
bin: 3.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34630
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2360
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 460
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5846
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 4.235493434985176e-4
allele num: 4722
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4400
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7636
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.73e-2

QD
type: SiteQuality
SIO_000300: 1.304e1

DP
type: SiteQuality
SIO_000300: 6.12838e5

MQRankSum
type: SiteQuality
SIO_000300: 7.47e-1

FS
type: SiteQuality
SIO_000300: 1.309e0

BaseQRankSum
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.231e0

GenotypeQuality
all individuals: 2984
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 395
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1177
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11737
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variant carriers: 0

GenotypeQuality
all individuals: 3557
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8113
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6124
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 5.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3708
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3018
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1630
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3604
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 4.038772213247173e-5
allele num: 24760
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5424
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.795e0

MQRankSum
type: SiteQuality
SIO_000300: -1.139e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.05e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.71e-2

FS
type: SiteQuality
SIO_000300: 5.237e0

DP
type: SiteQuality
SIO_000300: 5.3216e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.007e0

QD
type: SiteQuality
SIO_000300: 6.43e0

GenotypeQuality
all individuals: 4009
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2982
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 413
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1981
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1433
bin: 9.75e1
variant carriers: 23

GenotypeQuality
all individuals: 297
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variant carriers: 0

GenotypeQuality
all individuals: 1136
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 117
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variant carriers: 0

GenotypeQuality
all individuals: 229
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variant carriers: 0

GenotypeQuality
all individuals: 2040
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variant carriers: 0

GenotypeQuality
all individuals: 437
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variant carriers: 1

GenotypeQuality
all individuals: 3962
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18881
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 2
allele frequency: 2.037489812550937e-4
allele num: 9816
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10874
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15624
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8160
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 22
allele frequency: 3.464130503243686e-4
allele num: 63508
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.77e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.843e0

VQSLOD
type: SiteQuality
SIO_000300: 1.75e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.2e-1

DP
type: SiteQuality
SIO_000300: 1.29687e6

FS
type: SiteQuality
SIO_000300: 2.05e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

QD
type: SiteQuality
SIO_000300: 1.155e1

GenotypeQuality
all individuals: 94
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3943
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2631
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2039
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3075
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23853
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 438
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3901
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6076
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 579
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1998
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1146
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1418
bin: 9.75e1
variant carriers: 3

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10910
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.054367745876604e-4
allele num: 9822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8172
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6234
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63604
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.44e-1

DP
type: SiteQuality
SIO_000300: 1.320352e6

VQSLOD
type: SiteQuality
SIO_000300: 1.12e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.19e0

FS
type: SiteQuality
SIO_000300: 4.708e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 4.95e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.08e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.645e1

GenotypeQuality
all individuals: 4042
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3580
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 236
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 1419
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 87
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27525
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2061
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 890
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2115
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2388
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 458
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9836
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8188
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.568479829349395e-5
allele num: 63756
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10928
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15730
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

MQ
type: SiteQuality
SIO_000300: 5.878e1

VQSLOD
type: SiteQuality
SIO_000300: -2.942e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.157e0

DP
type: SiteQuality
SIO_000300: 1.349528e6

QD
type: SiteQuality
SIO_000300: 3.55e0

GenotypeQuality
all individuals: 1873
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2986
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2131
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28146
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2072
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 573
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3524
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2158
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 590
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 843
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6418
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1220
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3888
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1798
bin: 2.75e1
variant carriers: 0

Other
type: Population
allele count: 1
allele frequency: 1.152073732718894e-3
allele num: 868
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6248
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10936
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8196
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63784
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.409e0

MQRankSum
type: SiteQuality
SIO_000300: -6.3e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.232e0

DP
type: SiteQuality
SIO_000300: 1.355025e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

MQ
type: SiteQuality
SIO_000300: 5.907e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.840000000000001e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.12e0

QD
type: SiteQuality
SIO_000300: 7.98e0

GenotypeQuality
all individuals: 2089
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 464
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1725
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3432
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1742
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3710
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 5.75e1
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GenotypeQuality
all individuals: 855
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 595
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 7.75e1
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GenotypeQuality
all individuals: 1221
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6489
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1986
bin: 4.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8202
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15734
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.6e-4
allele num: 6250
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9864
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.408715251690458e-4
allele num: 63888
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10944
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.49e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.68e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.873e0

QD
type: SiteQuality
SIO_000300: 1.292e1

DP
type: SiteQuality
SIO_000300: 1.360832e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.4e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.4e-3

GenotypeQuality
all individuals: 32026
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6794
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 577
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1199
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2729
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
all individuals: 1102
bin: 4.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9884
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15774
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.122658006495129e-5
allele num: 64048
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6260
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11006
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.14e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.67e-1

FS
type: SiteQuality
SIO_000300: 9.215999999999999e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.403363e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.256e0

VQSLOD
type: SiteQuality
SIO_000300: -5.366e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.517e1

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1
allele frequency: 6.328312871788382e-5
allele num: 15802
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6272
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9908
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11022
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8264
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64140
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 2.09e1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.411345e6

MQRankSum
type: SiteQuality
SIO_000300: 2.21e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.33e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

GenotypeQuality
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bin: 2.75e1
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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variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64282
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.053050878145935e-5
allele num: 11046
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9920
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8288
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6278
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 6.019e0

MQRankSum
type: SiteQuality
SIO_000300: -9.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.738e-1

DP
type: SiteQuality
SIO_000300: 1.426106e6

BaseQRankSum
type: SiteQuality
SIO_000300: -1.269e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 8.69e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 3

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6284
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15876
num of homozygotes: 0

Other
type: Population
allele count: 3
allele frequency: 3.456221198156682e-3
allele num: 868
num of homozygotes: 0

Latino
type: Population
allele count: 21
allele frequency: 1.893939393939394e-3
allele num: 11088
num of homozygotes: 0

African
type: Population
allele count: 628
allele frequency: 6.285028022417935e-2
allele num: 9992
num of homozygotes: 14

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 1.706325815158378e-4
allele num: 64466
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8314
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.531e0

MQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

FS
type: SiteQuality
SIO_000300: 1.338e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.91e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.89e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.454276e6

QD
type: SiteQuality
SIO_000300: 1.352e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.94e-1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2271
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.54832316601121e-5
allele num: 64586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10034
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.512247205124984e-4
allele num: 15922
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.67e-1

DP
type: SiteQuality
SIO_000300: 1.456412e6

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.543e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.05e0

MQRankSum
type: SiteQuality
SIO_000300: 4.63e-1

QD
type: SiteQuality
SIO_000300: 1.442e1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15922
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.54832316601121e-5
allele num: 64586
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8346
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6306
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.456412e6

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

FS
type: SiteQuality
SIO_000300: 1.543e0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11180
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.926543577526305e-5
allele num: 10074
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16026
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64846
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.209e0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6348
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64846
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8408
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
allele count: 11
allele frequency: 6.863846249844003e-4
allele num: 16026
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.944543828264758e-5
allele num: 11180
num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 880
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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MQ
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2390
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10088
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.180637544273908e-4
allele num: 8470
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11224
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16100
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65052
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.2e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.54e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.982e0

DP
type: SiteQuality
SIO_000300: 1.486706e6

FS
type: SiteQuality
SIO_000300: 1.596e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.12e0

MQRankSum
type: SiteQuality
SIO_000300: -1.031e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.09e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8530
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16194
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11292
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6444
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10138
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.531675039823551e-5
allele num: 65288
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -3.21e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

MQ
type: SiteQuality
SIO_000300: 6.08e1

QD
type: SiteQuality
SIO_000300: 1.651e1

VQSLOD
type: SiteQuality
SIO_000300: 1.9e0

FS
type: SiteQuality
SIO_000300: 4.607e0

DP
type: SiteQuality
SIO_000300: 1.501464e6

ClippingRankSum
type: SiteQuality
SIO_000300: 6.66e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.4e-2

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8534
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10140
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11298
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6448
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 888
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.233501911927963e-4
allele num: 16214
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.6e-2

QD
type: SiteQuality
SIO_000300: 1.485e1

VQSLOD
type: SiteQuality
SIO_000300: 3.38e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.77e0

DP
type: SiteQuality
SIO_000300: 1.504055e6

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: 16

GenotypeQuality
all individuals: 1456
bin: 8.25e1
variant carriers: 1

African
type: Population
allele count: 12
allele frequency: 1.182732111176819e-3
allele num: 10146
num of homozygotes: 0

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

Latino
type: Population
allele count: 3
allele frequency: 2.654867256637168e-4
allele num: 11300
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.060162800660995e-5
allele num: 65356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6450
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16242
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.95e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.75e0

DP
type: SiteQuality
SIO_000300: 1.507643e6

FS
type: SiteQuality
SIO_000300: 1.24e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

MQRankSum
type: SiteQuality
SIO_000300: -7.099999999999999e-2

QD
type: SiteQuality
SIO_000300: 1.307e1

MQ
type: SiteQuality
SIO_000300: 5.984e1

GenotypeQuality
all individuals: 528
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 111

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1469
bin: 8.25e1
variant carriers: 2

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 104
allele frequency: 1.589825119236884e-3
allele num: 65416
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.967729240456513e-4
allele num: 10164
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.652989034311992e-4
allele num: 11308
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.093102381688834e-4
allele num: 6466
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.148548942449582e-5
allele num: 16264
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.123595505617978e-3
allele num: 890
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.03e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.33e0

MQRankSum
type: SiteQuality
SIO_000300: 1.94e-1

QD
type: SiteQuality
SIO_000300: 1.351e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.51e0

DP
type: SiteQuality
SIO_000300: 1.511617e6

GenotypeQuality
all individuals: 185
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: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10164
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65416
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11308
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.148548942449582e-5
allele num: 16264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6466
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 5.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

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

DP
type: SiteQuality
SIO_000300: 1.511617e6

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6514
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11370
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16328
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.524157902758726e-5
allele num: 65610
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.036e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

FS
type: SiteQuality
SIO_000300: 1.291e0

InbreedingCoeff
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SIO_000300: 2.0e-4

QD
type: SiteQuality
SIO_000300: 1.28e1

DP
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ReadPosRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: 3.59e0

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: 0
allele frequency: 0.0e0
allele num: 65868
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8622
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African
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11474
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South Asian
type: Population
allele count: 1
allele frequency: 6.085686465433301e-5
allele num: 16432
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6564
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.151e0

VQSLOD
type: SiteQuality
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MQRankSum
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InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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DP
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SIO_000300: 1.533438e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.17e-1

QD
type: SiteQuality
SIO_000300: 1.196e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 1386
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65956
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.076810889645114e-5
allele num: 16456
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.77e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

DP
type: SiteQuality
SIO_000300: 1.536664e6

QD
type: SiteQuality
SIO_000300: 1.292e1

FS
type: SiteQuality
SIO_000300: 4.948e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.842e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 1386
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 6.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65956
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.748488984207447e-5
allele num: 10258
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.948e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.77e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.55e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.842e0

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.536664e6

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.77e-1

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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.073120369245719e-5
allele num: 16466
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10262
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65964
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8628
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.05e0

VQSLOD
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

MQRankSum
type: SiteQuality
SIO_000300: -1.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 1.538065e6

FS
type: SiteQuality
SIO_000300: 2.969e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.59e-1

QD
type: SiteQuality
SIO_000300: 1.33e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 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: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2604
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16466
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6572
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.368e0

MQRankSum
type: SiteQuality
SIO_000300: -1.326e0

DP
type: SiteQuality
SIO_000300: 1.538483e6

FS
type: SiteQuality
SIO_000300: 1.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.45e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -9.45e-1

QD
type: SiteQuality
SIO_000300: 1.369e1

MQ
type: SiteQuality
SIO_000300: 5.97e1

GenotypeQuality
all individuals: 41
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 51
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variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 4.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6574
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21447656060238e-4
allele num: 16468
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65966
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10264
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.269e1

FS
type: SiteQuality
SIO_000300: 5.37e0

VQSLOD
type: SiteQuality
SIO_000300: 7.7e-1

DP
type: SiteQuality
SIO_000300: 1.538592e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.095e0

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 2.97e-1

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.25e1
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: 16482
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10276
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515518913676043e-5
allele num: 65984
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6580
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.969e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-1

FS
type: SiteQuality
SIO_000300: 2.662e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

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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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

South Asian
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allele count: 1
allele frequency: 6.066488716330988e-5
allele num: 16484
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66004
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.541869e6

MQ
type: SiteQuality
SIO_000300: 5.972e1

QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQRankSum
type: SiteQuality
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BaseQRankSum
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GenotypeQuality
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variant carriers: 1

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66004
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16484
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10278
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.673026886383348e-5
allele num: 11530
num of homozygotes: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6584
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MQRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.972e1

DP
type: SiteQuality
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ReadPosRankSum
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SIO_000300: 1.24e0

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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variant carriers: 126

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.72762645914397e-5
allele num: 10280
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 24
allele frequency: 3.6360330879011e-4
allele num: 66006
num of homozygotes: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.108647450110865e-3
allele num: 902
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.467406380027739e-4
allele num: 11536
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

South Asian
type: Population
allele count: 96
allele frequency: 5.821710127349909e-3
allele num: 16490
num of homozygotes: 1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.79e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.316e1

MQRankSum
type: SiteQuality
SIO_000300: 1.07e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

VQSLOD
type: SiteQuality
SIO_000300: 5.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.04e0

DP
type: SiteQuality
SIO_000300: 1.548664e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.83e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2596
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515197430225158e-5
allele num: 65998
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6588
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.474635163307853e-4
allele num: 8634
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11534
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.723842862699339e-5
allele num: 10284
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 902
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -5.11e-1

DP
type: SiteQuality
SIO_000300: 1.546426e6

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.72e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.7e0

VQSLOD
type: SiteQuality
SIO_000300: 1.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.401e1

MQ
type: SiteQuality
SIO_000300: 5.967e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.75e1
variant carriers: 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: 1
allele frequency: 6.064281382656155e-5
allele num: 16490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65994
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10286
num of homozygotes: 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: 11540
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.34e-1

QD
type: SiteQuality
SIO_000300: 1.035e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -6.48e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.070000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.546454e6

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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variant carriers: 0

East Asian
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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: 11542
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514967882680887e-5
allele num: 66008
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16488
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 1.546656e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.87e0

MQ
type: SiteQuality
SIO_000300: 5.965e1

MQRankSum
type: SiteQuality
SIO_000300: -9.1e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.66e0

QD
type: SiteQuality
SIO_000300: 1.383e1

VQSLOD
type: SiteQuality
SIO_000300: 5.73e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.02e-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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variant carriers: 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: 1.515059693351918e-5
allele num: 66004
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6596
num of homozygotes: 0

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

African
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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: 8636
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.6e-3

DP
type: SiteQuality
SIO_000300: 1.546545e6

FS
type: SiteQuality
SIO_000300: 7.971e0

VQSLOD
type: SiteQuality
SIO_000300: -1.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.7e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

MQRankSum
type: SiteQuality
SIO_000300: 1.72e0

QD
type: SiteQuality
SIO_000300: 9.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.7e-1

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
all individuals: 59
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GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514508996183437e-5
allele num: 66028
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
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MQ
type: SiteQuality
SIO_000300: 5.919e1

DP
type: SiteQuality
SIO_000300: 1.546901e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.757e1

FS
type: SiteQuality
SIO_000300: 1.126e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.49e-1

GenotypeQuality
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variant carriers: 0

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

Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66028
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.721952167995334e-5
allele num: 10286
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11542
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.84e-1

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQ
type: SiteQuality
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VQSLOD
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ReadPosRankSum
type: SiteQuality
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MQRankSum
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FS
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.546901e6

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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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6592
num of homozygotes: 0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10282
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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11540
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66012
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.276e0

BaseQRankSum
type: SiteQuality
SIO_000300: -7.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.42e-1

InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.546972e6

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 4.4e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6594
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

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
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African
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Other
type: Population
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European (Non-Finnish)
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allele count: 2
allele frequency: 3.029476809355024e-5
allele num: 66018
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

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

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

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.664009703690868e-5
allele num: 11542
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.514738404677512e-5
allele num: 66018
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.547359e6

MQRankSum
type: SiteQuality
SIO_000300: 1.96e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

FS
type: SiteQuality
SIO_000300: 3.514e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.7e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

QD
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SIO_000300: 1.252e1

BaseQRankSum
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SIO_000300: 2.48e0

GenotypeQuality
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bin: 8.25e1
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.027642374882679e-5
allele num: 66058
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.549823e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.434e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.93e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.17e0

FS
type: SiteQuality
SIO_000300: 7.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 6.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 9.46e-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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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: 11546
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 3.027275754548482e-5
allele num: 66066
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10302
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6600
num of homozygotes: 0

South Asian
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allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.08e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.78e-1

MQ
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SIO_000300: 5.906e1

FS
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

DP
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InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.63e-1

MQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.374e1

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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GenotypeQuality
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variant carriers: 1

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159285879897983e-4
allele num: 8626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 9
allele frequency: 1.367989056087551e-4
allele num: 65790
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.773260359655981e-5
allele num: 10232
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 7.713668620796051e-4
allele num: 6482
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 2.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.991e0

MQ
type: SiteQuality
SIO_000300: 5.927e1

MQRankSum
type: SiteQuality
SIO_000300: 1.67e-1

FS
type: SiteQuality
SIO_000300: 1.76571e2

BaseQRankSum
type: SiteQuality
SIO_000300: -3.696e0

VQSLOD
type: SiteQuality
SIO_000300: -1.467e2

QD
type: SiteQuality
SIO_000300: 2.5e-1

DP
type: SiteQuality
SIO_000300: 1.557051e6

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.512996641147457e-5
allele num: 66094
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10306
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -9.52e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

MQRankSum
type: SiteQuality
SIO_000300: -5.12e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.057e1

DP
type: SiteQuality
SIO_000300: 1.550487e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.66e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.12e-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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.51267622678042e-5
allele num: 66108
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -2.14e-1

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.123e0

DP
type: SiteQuality
SIO_000300: 1.551434e6

InbreedingCoeff
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SIO_000300: -4.0e-4

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.943e1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.23e0

GenotypeQuality
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variant carriers: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66108
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.227e0

VQSLOD
type: SiteQuality
SIO_000300: 7.85e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.551322e6

BaseQRankSum
type: SiteQuality
SIO_000300: 9.27e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.6e-1

QD
type: SiteQuality
SIO_000300: 1.328e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.07e-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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.025443983904638e-5
allele num: 66106
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.659508139937652e-5
allele num: 11548
num of homozygotes: 0

African
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allele count: 4
allele frequency: 3.881987577639751e-4
allele num: 10304
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East Asian
type: Population
allele count: 1
allele frequency: 1.157407407407407e-4
allele num: 8640
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6602
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Other
type: Population
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allele frequency: 0.0e0
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ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-2

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.538440591812653e-5
allele num: 66102
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.2073e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.1e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.938e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.59e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.9e-1

DP
type: SiteQuality
SIO_000300: 1.552113e6

VQSLOD
type: SiteQuality
SIO_000300: -1.544e0

MQRankSum
type: SiteQuality
SIO_000300: 7.69e-1

QD
type: SiteQuality
SIO_000300: 1.138e1

GenotypeQuality
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bin: 7.75e1
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: 9.75e1
variant carriers: 2

GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 5.25e1
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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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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10308
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66100
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

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

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

Latino
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allele count: 2
allele frequency: 1.731601731601732e-4
allele num: 11550
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.003e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.97e-1

DP
type: SiteQuality
SIO_000300: 1.551844e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.81e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.17e0

VQSLOD
type: SiteQuality
SIO_000300: 6.02e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10310
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6606
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.512630464377553e-5
allele num: 66110
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 4.046e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.56e-1

ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.952e1

MQRankSum
type: SiteQuality
SIO_000300: 8.03e-1

BaseQRankSum
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QD
type: SiteQuality
SIO_000300: 1.356e1

DP
type: SiteQuality
SIO_000300: 1.55238e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.42e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 3

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10304
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.597852441981296e-4
allele num: 11548
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66130
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 904
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16506
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

QD
type: SiteQuality
SIO_000300: 1.244e1

FS
type: SiteQuality
SIO_000300: 2.346e0

DP
type: SiteQuality
SIO_000300: 1.552643e6

MQ
type: SiteQuality
SIO_000300: 5.943e1

VQSLOD
type: SiteQuality
SIO_000300: 9.45e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.67e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.966e0

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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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66130
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6604
num of homozygotes: 0

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

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

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

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

Other
type: Population
allele count: 0
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allele num: 904
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.5e-2

FS
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
type: SiteQuality
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QD
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.966e0

VQSLOD
type: SiteQuality
SIO_000300: 9.45e-1

MQ
type: SiteQuality
SIO_000300: 5.943e1