2-190569836-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569836
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569836
    reference: chr 2
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1828C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1796C>T
  hgvsp: ENSP00000397243.2:p.Ser599Phe
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1796C>T
  hgvsp: ENSP00000313513.4:p.Ser599Phe
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1796C>T
  hgvsp: ENSP00000427882.1:p.Ser599Phe
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1583C>T
  hgvsp: ENSP00000393043.2:p.Ser528Phe
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1088C>T
  hgvsp: ENSP00000281412.6:p.Ser363Phe
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1088C>T
  hgvsp: ENSP00000407459.1:p.Ser363Phe
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1583C>T
  hgvsp: ENSP00000399928.2:p.Ser528Phe
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8223
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9426
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8245
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14243
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3911
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2720
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Ser599Phe
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

2-190569838-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569838
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569837
    reference: chr 2
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1096delA
  hgvsp: ENSP00000281412.6:p.Arg366GlufsTer29
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1804delA
  hgvsp: ENSP00000313513.4:p.Arg602GlufsTer29
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1820delA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1804delA
  hgvsp: ENSP00000397243.2:p.Arg602GlufsTer29
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1591delA
  hgvsp: ENSP00000399928.2:p.Arg531GlufsTer29
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1591delA
  hgvsp: ENSP00000393043.2:p.Arg531GlufsTer29
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1096delA
  hgvsp: ENSP00000407459.1:p.Arg366GlufsTer29
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1804delA
  hgvsp: ENSP00000427882.1:p.Arg602GlufsTer29
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1459
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8223
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14246
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3911
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg602GlufsTer29
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
population: East Asian
reference allele: GA
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-190569840-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569840
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569840
    reference: chr 2
allele count: 3
allele frequency: 2.471861971227527e-5
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1587A>G
  hgvsp: ENST00000433782.2:c.1587A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1800A>G
  hgvsp: ENST00000438402.2:c.1800A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1092A>G
  hgvsp: ENST00000441800.1:c.1092A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1092A>G
  hgvsp: ENST00000281412.6:c.1092A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1587A>G
  hgvsp: ENST00000431575.2:c.1587A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1800A>G
  hgvsp: ENST00000313581.4:c.1800A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1800A>G
  hgvsp: ENST00000520309.1:c.1800A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1824A>G
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 599
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3895
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1554
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4260
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Glu600Glu
num of homozygotes: 0
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: DP

2-190569845-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569845
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569845
    reference: chr 2
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1805G>T
  hgvsp: ENSP00000313513.4:p.Arg602Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1805G>T
  hgvsp: ENSP00000427882.1:p.Arg602Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1097G>T
  hgvsp: ENSP00000281412.6:p.Arg366Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1805G>T
  hgvsp: ENSP00000397243.2:p.Arg602Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1097G>T
  hgvsp: ENSP00000407459.1:p.Arg366Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1592G>T
  hgvsp: ENSP00000399928.2:p.Arg531Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1592G>T
  hgvsp: ENSP00000393043.2:p.Arg531Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1819G>T
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14245
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Arg602Ile
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff

2-190569847-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569847
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569847
    reference: chr 2
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1594G>A
  hgvsp: ENSP00000393043.2:p.Gly532Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1099G>A
  hgvsp: ENSP00000407459.1:p.Gly367Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1807G>A
  hgvsp: ENSP00000397243.2:p.Gly603Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1807G>A
  hgvsp: ENSP00000313513.4:p.Gly603Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1807G>A
  hgvsp: ENSP00000427882.1:p.Gly603Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1817G>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1594G>A
  hgvsp: ENSP00000399928.2:p.Gly532Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1099G>A
  hgvsp: ENSP00000281412.6:p.Gly367Ser
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5987
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14246
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31937
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2088
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gly603Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD

2-190569848-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569848
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569848
    reference: chr 2
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1816G>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1595G>A
  hgvsp: ENSP00000393043.2:p.Gly532Asp
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1595G>A
  hgvsp: ENSP00000399928.2:p.Gly532Asp
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1808G>A
  hgvsp: ENSP00000313513.4:p.Gly603Asp
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1100G>A
  hgvsp: ENSP00000281412.6:p.Gly367Asp
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1808G>A
  hgvsp: ENSP00000397243.2:p.Gly603Asp
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1100G>A
  hgvsp: ENSP00000407459.1:p.Gly367Asp
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1808G>A
  hgvsp: ENSP00000427882.1:p.Gly603Asp
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 600
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9425
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2715
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 4261
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly603Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum

2-190569851-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569851
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569851
    reference: chr 2
allele count: 2
allele frequency: 1.647826516824309e-5
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1811G>A
  hgvsp: ENSP00000427882.1:p.Trp604Ter
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1598G>A
  hgvsp: ENSP00000393043.2:p.Trp533Ter
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1813G>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1598G>A
  hgvsp: ENSP00000399928.2:p.Trp533Ter
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1103G>A
  hgvsp: ENSP00000281412.6:p.Trp368Ter
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1811G>A
  hgvsp: ENSP00000397243.2:p.Trp604Ter
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1811G>A
  hgvsp: ENSP00000313513.4:p.Trp604Ter
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1103G>A
  hgvsp: ENSP00000407459.1:p.Trp368Ter
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9424
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9904
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2088
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 679
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Trp604Ter
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum

2-190569852-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569852
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569852
    reference: chr 2
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1812G>T
  hgvsp: ENSP00000397243.2:p.Trp604Cys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1812G>T
  hgvsp: ENSP00000427882.1:p.Trp604Cys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1599G>T
  hgvsp: ENSP00000393043.2:p.Trp533Cys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1599G>T
  hgvsp: ENSP00000399928.2:p.Trp533Cys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1812G>T
  hgvsp: ENSP00000313513.4:p.Trp604Cys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1104G>T
  hgvsp: ENSP00000407459.1:p.Trp368Cys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1812G>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1104G>T
  hgvsp: ENSP00000281412.6:p.Trp368Cys
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8253
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9904
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14249
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Trp604Cys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP

2-190569855-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569855
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569855
    reference: chr 2
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1815G>A
  hgvsp: ENSP00000397243.2:p.Met605Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1602G>A
  hgvsp: ENSP00000393043.2:p.Met534Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1602G>A
  hgvsp: ENSP00000399928.2:p.Met534Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1107G>A
  hgvsp: ENSP00000407459.1:p.Met369Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1815G>A
  hgvsp: ENSP00000313513.4:p.Met605Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1815G>A
  hgvsp: ENSP00000427882.1:p.Met605Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1809G>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1107G>A
  hgvsp: ENSP00000281412.6:p.Met369Ile
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9906
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5985
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2452
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9423
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5747
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1556
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1460
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8220
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 350
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4260
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2088
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Met605Ile
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: MQ

2-190569858-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569858
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569858
    reference: chr 2
allele count: 39
allele frequency: 3.2133146576584e-4
allele num: 121370
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1818G>A
  hgvsp: ENST00000438402.2:c.1818G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1605G>A
  hgvsp: ENST00000431575.2:c.1605G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1605G>A
  hgvsp: ENST00000433782.2:c.1605G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1818G>A
  hgvsp: ENST00000520309.1:c.1818G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1110G>A
  hgvsp: ENST00000441800.1:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1110G>A
  hgvsp: ENST00000281412.6:c.1110G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1818G>A
  hgvsp: ENST00000313581.4:c.1818G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1806G>A
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1063
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1555
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3894
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 520
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 353
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 9.75e1
  variant carriers: 34
genotype depth: GenotypeDepth
  all individuals: 9419
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5744
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 797
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2725
  bin: 9.75e1
  variant carriers: 39
genotype quality: GenotypeQuality
  all individuals: 824
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3910
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro606Pro
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

2-190569870-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569870
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569870
    reference: chr 2
allele count: 3
allele frequency: 2.471780505891077e-5
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1617C>T
  hgvsp: ENST00000433782.2:c.1617C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1830C>T
  hgvsp: ENST00000438402.2:c.1830C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1830C>T
  hgvsp: ENST00000313581.4:c.1830C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1830C>T
  hgvsp: ENST00000520309.1:c.1830C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1122C>T
  hgvsp: ENST00000441800.1:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1122C>T
  hgvsp: ENST00000281412.6:c.1122C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1617C>T
  hgvsp: ENST00000431575.2:c.1617C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1794C>T
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5745
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8250
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1563
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1064
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9419
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14255
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3913
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ala610Ala
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

2-190569871-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569871
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569871
    reference: chr 2
allele count: 4
allele frequency: 3.295544423938835e-5
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1831G>A
  hgvsp: ENSP00000397243.2:p.Ala611Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1123G>A
  hgvsp: ENSP00000407459.1:p.Ala375Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1618G>A
  hgvsp: ENSP00000393043.2:p.Ala540Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1793G>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1618G>A
  hgvsp: ENSP00000399928.2:p.Ala540Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1123G>A
  hgvsp: ENSP00000281412.6:p.Ala375Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1831G>A
  hgvsp: ENSP00000313513.4:p.Ala611Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1831G>A
  hgvsp: ENSP00000427882.1:p.Ala611Thr
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1066
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5744
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1469
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14254
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4262
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 682
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ala611Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
population: African
population: Other
population: European (Finnish)
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

2-190569873-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569873
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569873
    reference: chr 2
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1833T>G
  hgvsp: ENST00000438402.2:c.1833T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1125T>G
  hgvsp: ENST00000281412.6:c.1125T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1791T>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1620T>G
  hgvsp: ENST00000431575.2:c.1620T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1833T>G
  hgvsp: ENST00000520309.1:c.1833T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1620T>G
  hgvsp: ENST00000433782.2:c.1620T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1125T>G
  hgvsp: ENST00000441800.1:c.1125T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1833T>G
  hgvsp: ENST00000313581.4:c.1833T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9901
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5980
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1067
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5745
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31966
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4261
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14254
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3914
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala611Ala
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: African
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

2-190569878-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569878
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569878
    reference: chr 2
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1625A>G
  hgvsp: ENSP00000393043.2:p.Tyr542Cys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1130A>G
  hgvsp: ENSP00000407459.1:p.Tyr377Cys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1625A>G
  hgvsp: ENSP00000399928.2:p.Tyr542Cys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1838A>G
  hgvsp: ENSP00000427882.1:p.Tyr613Cys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1130A>G
  hgvsp: ENSP00000281412.6:p.Tyr377Cys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1786A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1838A>G
  hgvsp: ENSP00000313513.4:p.Tyr613Cys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1838A>G
  hgvsp: ENSP00000397243.2:p.Tyr613Cys
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5981
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2451
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 447
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9416
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5745
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9900
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 823
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Tyr613Cys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: East Asian
population: Other
reference allele: A
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

http://identifiers.org/exac.variant/2-190569885-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569885
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569885
    reference: chr 2
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1845C>A
  hgvsp: ENSP00000313513.4:p.Asn615Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1779C>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1845C>A
  hgvsp: ENSP00000397243.2:p.Asn615Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1632C>A
  hgvsp: ENSP00000399928.2:p.Asn544Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1137C>A
  hgvsp: ENSP00000407459.1:p.Asn379Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1845C>A
  hgvsp: ENSP00000427882.1:p.Asn615Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1632C>A
  hgvsp: ENSP00000393043.2:p.Asn544Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1137C>A
  hgvsp: ENSP00000281412.6:p.Asn379Lys
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9890
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8216
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31967
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Asn615Lys
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum

2-190569885-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569885
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569885
    reference: chr 2
allele count: 45
allele frequency: 3.707365299060801e-4
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1632C>T
  hgvsp: ENST00000431575.2:c.1632C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1137C>T
  hgvsp: ENST00000281412.6:c.1137C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1845C>T
  hgvsp: ENST00000438402.2:c.1845C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1779C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1137C>T
  hgvsp: ENST00000441800.1:c.1137C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1632C>T
  hgvsp: ENST00000433782.2:c.1632C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1845C>T
  hgvsp: ENST00000313581.4:c.1845C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1845C>T
  hgvsp: ENST00000520309.1:c.1845C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8216
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9890
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3897
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 352
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1564
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2448
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 9.75e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 3913
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2082
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2707
  bin: 9.75e1
  variant carriers: 45
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asn615Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum

2-190569886-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569886
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569886
    reference: chr 2
allele count: 3
allele frequency: 2.47161759132627e-5
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1846G>A
  hgvsp: ENSP00000397243.2:p.Val616Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1633G>A
  hgvsp: ENSP00000393043.2:p.Val545Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1846G>A
  hgvsp: ENSP00000313513.4:p.Val616Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1138G>A
  hgvsp: ENSP00000281412.6:p.Val380Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1633G>A
  hgvsp: ENSP00000399928.2:p.Val545Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1138G>A
  hgvsp: ENSP00000407459.1:p.Val380Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1846G>A
  hgvsp: ENSP00000427882.1:p.Val616Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1778G>A
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1470
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8248
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5971
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8222
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3906
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 521
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4262
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Val616Ile
num of homozygotes: 0
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum

2-190569894-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569894
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569894
    reference: chr 2
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1854C>G
  hgvsp: ENSP00000397243.2:p.Ile618Met
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1770C>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1146C>G
  hgvsp: ENSP00000281412.6:p.Ile382Met
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1641C>G
  hgvsp: ENSP00000399928.2:p.Ile547Met
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1854C>G
  hgvsp: ENSP00000313513.4:p.Ile618Met
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1641C>G
  hgvsp: ENSP00000393043.2:p.Ile547Met
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1146C>G
  hgvsp: ENSP00000407459.1:p.Ile382Met
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1854C>G
  hgvsp: ENSP00000427882.1:p.Ile618Met
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31993
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile618Met
num of homozygotes: 0
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD

2-190569899-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569899
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569899
    reference: chr 2
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1859T>C
  hgvsp: ENSP00000313513.4:p.Ile620Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1151T>C
  hgvsp: ENSP00000407459.1:p.Ile384Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1646T>C
  hgvsp: ENSP00000399928.2:p.Ile549Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1151T>C
  hgvsp: ENSP00000281412.6:p.Ile384Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1646T>C
  hgvsp: ENSP00000393043.2:p.Ile549Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1859T>C
  hgvsp: ENSP00000397243.2:p.Ile620Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1765T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1859T>C
  hgvsp: ENSP00000427882.1:p.Ile620Thr
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1569
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2659
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 31987
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14261
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 680
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ile620Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: QD

http://identifiers.org/exac.variant/2-190569902-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569902
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569902
    reference: chr 2
allele count: 4
allele frequency: 3.295544423938835e-5
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1862C>A
  hgvsp: ENSP00000313513.4:p.Ala621Asp
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1649C>A
  hgvsp: ENSP00000399928.2:p.Ala550Asp
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1862C>A
  hgvsp: ENSP00000397243.2:p.Ala621Asp
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1762C>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1154C>A
  hgvsp: ENSP00000281412.6:p.Ala385Asp
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1649C>A
  hgvsp: ENSP00000393043.2:p.Ala550Asp
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1154C>A
  hgvsp: ENSP00000407459.1:p.Ala385Asp
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1862C>A
  hgvsp: ENSP00000427882.1:p.Ala621Asp
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8247
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1070
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 799
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5975
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5748
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9890
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3906
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1471
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3917
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4259
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2081
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Ala621Asp
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum

2-190569903-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569903
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569903
    reference: chr 2
allele count: 1
allele frequency: 8.238996819747227e-6
allele num: 121374
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1650T>C
  hgvsp: ENST00000431575.2:c.1650T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1863T>C
  hgvsp: ENST00000520309.1:c.1863T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1761T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1155T>C
  hgvsp: ENST00000441800.1:c.1155T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1863T>C
  hgvsp: ENST00000438402.2:c.1863T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1863T>C
  hgvsp: ENST00000313581.4:c.1863T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1650T>C
  hgvsp: ENST00000433782.2:c.1650T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1155T>C
  hgvsp: ENST00000281412.6:c.1155T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1071
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 351
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8246
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2455
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1570
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5749
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3906
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9889
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1468
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5974
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 448
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8221
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 800
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala621Ala
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS

2-190569908-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569908
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569908
    reference: chr 2
allele count: 2157
allele frequency: 1.777122330609017e-2
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1868G>A
  hgvsp: ENSP00000397243.2:p.Cys623Tyr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1160G>A
  hgvsp: ENSP00000281412.6:p.Cys387Tyr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1160G>A
  hgvsp: ENSP00000407459.1:p.Cys387Tyr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1655G>A
  hgvsp: ENSP00000399928.2:p.Cys552Tyr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1655G>A
  hgvsp: ENSP00000393043.2:p.Cys552Tyr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1868G>A
  hgvsp: ENSP00000427882.1:p.Cys623Tyr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1868G>A
  hgvsp: ENSP00000313513.4:p.Cys623Tyr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1756G>A
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9553
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3259
  bin: 9.75e1
  variant carriers: 1855
genotype depth: GenotypeDepth
  all individuals: 390
  bin: 9.25e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 8.25e1
  variant carriers: 37
genotype depth: GenotypeDepth
  all individuals: 5751
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5582
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 6.75e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 7.25e1
  variant carriers: 25
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 5.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9077
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3769
  bin: 5.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 7968
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1522
  bin: 6.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 7941
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 481
  bin: 8.75e1
  variant carriers: 52
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 7.75e1
  variant carriers: 29
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 595
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1935
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys623Tyr
num of homozygotes: 34
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum

2-190569917-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569917
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569917
    reference: chr 2
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1169A>G
  hgvsp: ENSP00000407459.1:p.Asp390Gly
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1664A>G
  hgvsp: ENSP00000399928.2:p.Asp555Gly
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1664A>G
  hgvsp: ENSP00000393043.2:p.Asp555Gly
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1169A>G
  hgvsp: ENSP00000281412.6:p.Asp390Gly
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1877A>G
  hgvsp: ENSP00000397243.2:p.Asp626Gly
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1877A>G
  hgvsp: ENSP00000427882.1:p.Asp626Gly
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1877A>G
  hgvsp: ENSP00000313513.4:p.Asp626Gly
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1747A>G
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8008
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1582
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8168
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32863
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asp626Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

2-190569918-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569918
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569918
    reference: chr 2
allele count: 1
allele frequency: 8.239675686364985e-6
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1746T>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1170T>A
  hgvsp: ENSP00000281412.6:p.Asp390Glu
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1878T>A
  hgvsp: ENSP00000397243.2:p.Asp626Glu
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1878T>A
  hgvsp: ENSP00000427882.1:p.Asp626Glu
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1665T>A
  hgvsp: ENSP00000399928.2:p.Asp555Glu
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1878T>A
  hgvsp: ENSP00000313513.4:p.Asp626Glu
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1170T>A
  hgvsp: ENSP00000407459.1:p.Asp390Glu
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1665T>A
  hgvsp: ENSP00000393043.2:p.Asp555Glu
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5783
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1709
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5742
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4301
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32860
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp626Glu
num of homozygotes: 0
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: African
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

2-190569920-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569920
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569920
    reference: chr 2
allele count: 2
allele frequency: 1.647989452867502e-5
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1172C>G
  hgvsp: ENSP00000281412.6:p.Pro391Arg
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1744C>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1880C>G
  hgvsp: ENSP00000313513.4:p.Pro627Arg
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1172C>G
  hgvsp: ENSP00000407459.1:p.Pro391Arg
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1667C>G
  hgvsp: ENSP00000393043.2:p.Pro556Arg
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1667C>G
  hgvsp: ENSP00000399928.2:p.Pro556Arg
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1880C>G
  hgvsp: ENSP00000427882.1:p.Pro627Arg
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1880C>G
  hgvsp: ENSP00000397243.2:p.Pro627Arg
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5741
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8171
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8006
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32855
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Pro627Arg
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum

2-190569923-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569923
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569923
    reference: chr 2
allele count: 4
allele frequency: 3.295870274545994e-5
allele num: 121364
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1883G>A
  hgvsp: ENSP00000427882.1:p.Ser628Asn
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1883G>A
  hgvsp: ENSP00000397243.2:p.Ser628Asn
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1175G>A
  hgvsp: ENSP00000281412.6:p.Ser392Asn
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1670G>A
  hgvsp: ENSP00000393043.2:p.Ser557Asn
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1883G>A
  hgvsp: ENSP00000313513.4:p.Ser628Asn
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1741G>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1670G>A
  hgvsp: ENSP00000399928.2:p.Ser557Asn
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1175G>A
  hgvsp: ENSP00000407459.1:p.Ser392Asn
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8007
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8170
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2614
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1586
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 5739
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser628Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum

2-190569926-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569926
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569926
    reference: chr 2
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1886T>A
  hgvsp: ENSP00000427882.1:p.Leu629Ter
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1886T>A
  hgvsp: ENSP00000397243.2:p.Leu629Ter
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1886T>A
  hgvsp: ENSP00000313513.4:p.Leu629Ter
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1178T>A
  hgvsp: ENSP00000407459.1:p.Leu393Ter
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1673T>A
  hgvsp: ENSP00000399928.2:p.Leu558Ter
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1178T>A
  hgvsp: ENSP00000281412.6:p.Leu393Ter
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1673T>A
  hgvsp: ENSP00000393043.2:p.Leu558Ter
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1738T>A
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8169
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9639
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8004
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1222
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14637
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 709
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Leu629Ter
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum

2-190569928-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569928
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569928
    reference: chr 2
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1675C>T
  hgvsp: ENST00000433782.2:c.1675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1888C>T
  hgvsp: ENST00000520309.1:c.1888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1888C>T
  hgvsp: ENST00000438402.2:c.1888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1180C>T
  hgvsp: ENST00000441800.1:c.1180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1736C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1180C>T
  hgvsp: ENST00000281412.6:c.1180C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1675C>T
  hgvsp: ENST00000431575.2:c.1675C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1888C>T
  hgvsp: ENST00000313581.4:c.1888C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8001
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Leu630Leu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

2-190569930-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569930
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569930
    reference: chr 2
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1677A>G
  hgvsp: ENST00000431575.2:c.1677A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1890A>G
  hgvsp: ENST00000438402.2:c.1890A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1182A>G
  hgvsp: ENST00000441800.1:c.1182A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1890A>G
  hgvsp: ENST00000313581.4:c.1890A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1677A>G
  hgvsp: ENST00000433782.2:c.1677A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1734A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1182A>G
  hgvsp: ENST00000281412.6:c.1182A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1890A>G
  hgvsp: ENST00000520309.1:c.1890A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4020
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5731
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9641
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1533
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu630Leu
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

2-190569932-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569932
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569932
    reference: chr 2
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1184A>T
  hgvsp: ENSP00000281412.6:p.Glu395Val
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1892A>T
  hgvsp: ENSP00000313513.4:p.Glu631Val
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1184A>T
  hgvsp: ENSP00000407459.1:p.Glu395Val
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1732A>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1679A>T
  hgvsp: ENSP00000393043.2:p.Glu560Val
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1679A>T
  hgvsp: ENSP00000399928.2:p.Glu560Val
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1892A>T
  hgvsp: ENSP00000427882.1:p.Glu631Val
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1892A>T
  hgvsp: ENSP00000397243.2:p.Glu631Val
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7994
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4021
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9642
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5733
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2615
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32847
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Glu631Val
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

2-190569943-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569943
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569943
    reference: chr 2
allele count: 8
allele frequency: 6.592718342590609e-5
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1690A>T
  hgvsp: ENSP00000399928.2:p.Thr564Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1690A>T
  hgvsp: ENSP00000393043.2:p.Thr564Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1903A>T
  hgvsp: ENSP00000427882.1:p.Thr635Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1721A>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1195A>T
  hgvsp: ENSP00000407459.1:p.Thr399Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1195A>T
  hgvsp: ENSP00000281412.6:p.Thr399Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1903A>T
  hgvsp: ENSP00000313513.4:p.Thr635Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1903A>T
  hgvsp: ENSP00000397243.2:p.Thr635Ser
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9637
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1707
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7978
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5779
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2006
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr635Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ

2-190569944-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569944
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569944
    reference: chr 2
allele count: 7
allele frequency: 5.76881871075143e-5
allele num: 121342
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1196C>T
  hgvsp: ENSP00000407459.1:p.Thr399Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1904C>T
  hgvsp: ENSP00000397243.2:p.Thr635Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1904C>T
  hgvsp: ENSP00000313513.4:p.Thr635Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1904C>T
  hgvsp: ENSP00000427882.1:p.Thr635Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1196C>T
  hgvsp: ENSP00000281412.6:p.Thr399Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1720C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1691C>T
  hgvsp: ENSP00000399928.2:p.Thr564Ile
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1691C>T
  hgvsp: ENSP00000393043.2:p.Thr564Ile
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9230
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1710
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 472
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1589
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5720
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9636
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 614
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32826
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Thr635Ile
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

2-190569953-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569953
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569953
    reference: chr 2
allele count: 2
allele frequency: 1.648451280022419e-5
allele num: 121326
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1910+3A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1697+3A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1910+3A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1910+3A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1697+3A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1202+3A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1711A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1202+3A>G
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1585
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 8165
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9228
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7938
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9630
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1518
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 14626
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32775
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3987
  bin: 7.25e1
  variant carriers: 0
hgvs: c.1910+3A>G
num of homozygotes: 0
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Other
reference allele: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

2-190569967-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569967
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569967
    reference: chr 2
allele count: 1
allele frequency: 8.243751236562685e-6
allele num: 121304
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1202+17T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1697+17T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1910+17T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1697T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1697+17T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1910+17T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1910+17T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1202+17T>C
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5625
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1224
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9598
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7836
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8167
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9229
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 301
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3986
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: African
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

2-190569970-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569970
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569970
    reference: chr 2
allele count: 1
allele frequency: 8.244430886935875e-6
allele num: 121294
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1697+20T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1202+20T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1910+20T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1697+20T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1202+20T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1910+20T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1694T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1910+20T>C
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2616
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8166
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9593
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5612
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9231
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4019
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1714
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5778
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7829
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14595
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32572
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4298
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

2-190569984-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569984
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569984
    reference: chr 2
allele count: 2
allele frequency: 1.652810604432838e-5
allele num: 121006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1202+34T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1202+34T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1910+34T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1680T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1697+34T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1910+34T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1697+34T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1910+34T>C
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7754
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9477
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2617
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1225
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 396
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9206
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8154
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5782
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1583
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4027
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1277
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 196
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4283
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 612
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14416
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31407
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1503
  bin: 9.75e1
  variant carriers: 2
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

2-190569987-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569987
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569987
    reference: chr 2
allele count: 3
allele frequency: 2.483567064589301e-5
allele num: 120794
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1697+37T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1697+37T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1910+37T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1202+37T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1910+37T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1910+37T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1202+37T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1677T>C
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1713
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8148
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7976
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 897
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 359
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 204
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4018
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 542
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 672
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9640
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4230
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 305
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29859
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2794
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: DP

2-190569991-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569991
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569991
    reference: chr 2
allele count: 15
allele frequency: 1.260567759718978e-4
allele num: 118994
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1910+41T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1910+41T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1202+41T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1910+41T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1697+41T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1673T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1697+41T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1202+41T>C
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10223
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 356
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 7693
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10091
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3179
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1264
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 312
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2080
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5276
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1584
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8325
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 923
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2121
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1011
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4079
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum

2-190569994-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190569994
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569994
    reference: chr 2
allele count: 2
allele frequency: 1.736744299136838e-5
allele num: 115158
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1697+44G>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1910+44G>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1202+44G>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1670G>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1697+44G>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1910+44G>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1910+44G>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1202+44G>C
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1590
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 570
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 648
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3953
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5713
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8628
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7502
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1473
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7346
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1425
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8573
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 912
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2362
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6833
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2088
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 441
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7328
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1718
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2122
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5372
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

2-190570001-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190570001
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190570000
    reference: chr 2
allele count: 114764
allele frequency: 9.944887348353553e-1
allele num: 115400
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1910+61delA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1697+61delA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1653delA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1910+61delA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1697+61delA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1202+61delA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1910+61delA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1202+61delA
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 2.25e1
  variant carriers: 8654
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 169
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.25e1
  variant carriers: 273
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.75e1
  variant carriers: 819
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 235
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 4.25e1
  variant carriers: 4744
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 5.25e1
  variant carriers: 1659
genotype depth: GenotypeDepth
  all individuals: 6634
  bin: 1.75e1
  variant carriers: 6634
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.25e1
  variant carriers: 667
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.75e1
  variant carriers: 330
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 4.75e1
  variant carriers: 2814
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.25e1
  variant carriers: 435
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 1.25e1
  variant carriers: 3543
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 7.5e0
  variant carriers: 1233
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 6.75e1
  variant carriers: 537
genotype depth: GenotypeDepth
  all individuals: 9190
  bin: 3.25e1
  variant carriers: 9188
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 229
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 5.75e1
  variant carriers: 1105
genotype depth: GenotypeDepth
  all individuals: 7167
  bin: 3.75e1
  variant carriers: 7164
genotype depth: GenotypeDepth
  all individuals: 9989
  bin: 2.75e1
  variant carriers: 9986
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 1.75e1
  variant carriers: 691
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 1.25e1
  variant carriers: 545
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 3.25e1
  variant carriers: 1411
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 2.75e1
  variant carriers: 1160
genotype quality: GenotypeQuality
  all individuals: 3143
  bin: 8.25e1
  variant carriers: 3143
genotype quality: GenotypeQuality
  all individuals: 2349
  bin: 4.75e1
  variant carriers: 2347
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 2.5e0
  variant carriers: 266
genotype quality: GenotypeQuality
  all individuals: 3102
  bin: 5.75e1
  variant carriers: 3102
num of homozygotes: 57076
population: Other
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: TA
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

2-190570001-TAA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190570001
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190569999
    reference: chr 2
allele count: 71
allele frequency: 6.152512998266898e-4
allele num: 115400
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1910+60_1910+61delAA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1910+60_1910+61delAA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1697+60_1697+61delAA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1910+60_1910+61delAA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1697+60_1697+61delAA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1202+60_1202+61delAA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1202+60_1202+61delAA
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1654_70-1653delAA
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 6.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6634
  bin: 1.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 1.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 9989
  bin: 2.75e1
  variant carriers: 55
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9190
  bin: 3.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 2.25e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7167
  bin: 3.75e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 2.5e0
  variant carriers: 22
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 1.25e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 2692
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2428
  bin: 5.25e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 3274
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 7.5e0
  variant carriers: 21
genotype quality: GenotypeQuality
  all individuals: 1411
  bin: 3.25e1
  variant carriers: 9
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 2.25e1
  variant carriers: 19
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: East Asian
reference allele: TAA
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD

2-190570001-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190570001
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190570001
    reference: chr 2
allele count: 3
allele frequency: 2.599653379549393e-5
allele num: 115400
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1202+51T>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-1663T>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1202+51T>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1910+51T>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1910+51T>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1910+51T>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1697+51T>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1697+51T>A
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 273
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9989
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6634
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4747
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1236
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9190
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2814
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8654
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7167
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1107
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 322
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2105
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1575
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1161
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2863
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2692
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

2-190571623-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571623
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571623
    reference: chr 2
allele count: 1
allele frequency: 8.462671157524161e-6
allele num: 118166
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1911-41C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1203-41C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1698-41C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1203-41C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-41C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1911-41C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1698-41C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1911-41C>T
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14301
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11490
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1878
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22980
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3000
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2899
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1279
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1408
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 704
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 796
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1176
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

2-190571625-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571625
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571625
    reference: chr 2
allele count: 1
allele frequency: 8.452513777597457e-6
allele num: 118308
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1911-39C>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1698-39C>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1698-39C>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1911-39C>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1911-39C>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1203-39C>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1203-39C>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-39C>G
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1417
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2745
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23118
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1350
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11509
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41046
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1321
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2387
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 668
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

2-190571629-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571629
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571629
    reference: chr 2
allele count: 4
allele frequency: 3.374388392103931e-5
allele num: 118540
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1911-35A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1911-35A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1203-35A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1698-35A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1911-35A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1698-35A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1203-35A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-35A>G
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1306
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2900
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2234
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 863
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11512
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23323
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 258
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42268
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: South Asian
population: Other
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

2-190571632-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571632
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571632
    reference: chr 2
allele count: 6
allele frequency: 5.058254227857492e-5
allele num: 118618
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1698-32C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1911-32C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1203-32C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1203-32C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1911-32C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-32C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1698-32C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1911-32C>T
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11560
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 990
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16280
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1860
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1166
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 253
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 130
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 610
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/2-190571639-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571639
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571639
    reference: chr 2
allele count: 3
allele frequency: 2.516820752026041e-5
allele num: 119198
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1911-25A>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1911-25A>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1698-25A>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1911-25A>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-25A>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1203-25A>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1203-25A>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1698-25A>C
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1062
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2904
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1041
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17378
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1327
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1081
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 92
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2385
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 7487
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: QD

2-190571647-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571647
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571647
    reference: chr 2
allele count: 1
allele frequency: 8.351428094204109e-6
allele num: 119740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1911-17T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1203-17T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1698-17T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1698-17T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1911-17T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-17T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1911-17T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1203-17T>C
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17970
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 783
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11623
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 601
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45105
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 213
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP

2-190571649-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571649
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571649
    reference: chr 2
allele count: 2
allele frequency: 1.668613382279326e-5
allele num: 119860
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1911-15T>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1911-15T>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1911-15T>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1698-15T>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1698-15T>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1203-15T>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1203-15T>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-15T>G
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 150
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24016
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18044
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 672
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 135
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1331
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

2-190571651-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571651
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571651
    reference: chr 2
allele count: 9
allele frequency: 7.501125168775316e-5
allele num: 119982
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1911-13T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1698-13T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1911-13T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1203-13T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-13T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1911-13T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1203-13T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1698-13T>C
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 514
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2906
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11642
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18123
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24064
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 181
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7561
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1198
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1336
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: South Asian
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum

2-190571656-A-AT
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571656
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571657
    reference: chr 2
allele count: 1
allele frequency: 8.313104778372627e-6
allele num: 120292
alternate allele: AT
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1698-3dupT
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-3dupT
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1698-3dupT
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1911-3dupT
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1203-3dupT
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1911-3dupT
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1911-3dupT
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1203-3dupT
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24160
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2910
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11680
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 518
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 536
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 669
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 4.75e1
  variant carriers: 0
hgvs: c.1911-3dupT
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: A
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

2-190571657-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571657
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571657
    reference: chr 2
allele count: 1
allele frequency: 8.3099270388406e-6
allele num: 120338
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1698-7T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1203-7T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1698-7T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1911-7T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1203-7T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.70-7T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1911-7T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1911-7T>C
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 277
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 498
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11674
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18319
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 519
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45670
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
hgvs: c.1911-7T>C
num of homozygotes: 0
population: Other
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: T
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum

2-190571667-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571667
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571667
    reference: chr 2
allele count: 1
allele frequency: 8.279653579294243e-6
allele num: 120778
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.73T>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1914T>G
  hgvsp: ENSP00000313513.4:p.Asn638Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1914T>G
  hgvsp: ENSP00000427882.1:p.Asn638Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1914T>G
  hgvsp: ENSP00000397243.2:p.Asn638Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1701T>G
  hgvsp: ENSP00000399928.2:p.Asn567Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1206T>G
  hgvsp: ENSP00000281412.6:p.Asn402Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1206T>G
  hgvsp: ENSP00000407459.1:p.Asn402Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1701T>G
  hgvsp: ENSP00000393043.2:p.Asn567Lys
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 262
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18552
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11709
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46096
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2382
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asn638Lys
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: MQ

2-190571685-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571685
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571685
    reference: chr 2
allele count: 1
allele frequency: 8.257638315441784e-6
allele num: 121100
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1932A>G
  hgvsp: ENST00000313581.4:c.1932A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1224A>G
  hgvsp: ENST00000281412.6:c.1224A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1224A>G
  hgvsp: ENST00000441800.1:c.1224A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.91A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1719A>G
  hgvsp: ENST00000433782.2:c.1719A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1719A>G
  hgvsp: ENST00000431575.2:c.1719A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1932A>G
  hgvsp: ENST00000520309.1:c.1932A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1932A>G
  hgvsp: ENST00000438402.2:c.1932A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 141
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 513
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18511
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 276
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2914
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 676
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 71
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7662
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu644Leu
num of homozygotes: 0
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

2-190571689-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571689
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571689
    reference: chr 2
allele count: 8
allele frequency: 6.606328863050802e-5
allele num: 121096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1723G>A
  hgvsp: ENSP00000399928.2:p.Ala575Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.95G>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1228G>A
  hgvsp: ENSP00000281412.6:p.Ala410Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1228G>A
  hgvsp: ENSP00000407459.1:p.Ala410Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1936G>A
  hgvsp: ENSP00000397243.2:p.Ala646Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1723G>A
  hgvsp: ENSP00000393043.2:p.Ala575Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1936G>A
  hgvsp: ENSP00000427882.1:p.Ala646Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1936G>A
  hgvsp: ENSP00000313513.4:p.Ala646Thr
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2918
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11771
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18513
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 4.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1343
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala646Thr
num of homozygotes: 1
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

2-190571691-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571691
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571691
    reference: chr 2
allele count: 1
allele frequency: 8.253685270473266e-6
allele num: 121158
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1230T>C
  hgvsp: ENST00000281412.6:c.1230T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1725T>C
  hgvsp: ENST00000433782.2:c.1725T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1938T>C
  hgvsp: ENST00000313581.4:c.1938T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1938T>C
  hgvsp: ENST00000438402.2:c.1938T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1725T>C
  hgvsp: ENST00000431575.2:c.1725T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1230T>C
  hgvsp: ENST00000441800.1:c.1230T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.97T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1938T>C
  hgvsp: ENST00000520309.1:c.1938T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24650
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11782
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18522
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2363
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala646Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

2-190571692-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571692
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571692
    reference: chr 2
allele count: 45
allele frequency: 3.713851842070514e-4
allele num: 121168
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.98G>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1231G>A
  hgvsp: ENSP00000281412.6:p.Ala411Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1939G>A
  hgvsp: ENSP00000313513.4:p.Ala647Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1939G>A
  hgvsp: ENSP00000397243.2:p.Ala647Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1726G>A
  hgvsp: ENSP00000399928.2:p.Ala576Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1939G>A
  hgvsp: ENSP00000427882.1:p.Ala647Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1231G>A
  hgvsp: ENSP00000407459.1:p.Ala411Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1726G>A
  hgvsp: ENSP00000393043.2:p.Ala576Thr
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11778
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18516
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 9.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 24646
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2911
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 269
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46486
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1346
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 263
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Ala647Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

2-190571700-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571700
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571700
    reference: chr 2
allele count: 2
allele frequency: 1.650437365901964e-5
allele num: 121180
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1947A>G
  hgvsp: ENST00000438402.2:c.1947A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1734A>G
  hgvsp: ENST00000433782.2:c.1734A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1239A>G
  hgvsp: ENST00000281412.6:c.1239A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.106A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1239A>G
  hgvsp: ENST00000441800.1:c.1239A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1947A>G
  hgvsp: ENST00000313581.4:c.1947A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1734A>G
  hgvsp: ENST00000431575.2:c.1734A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1947A>G
  hgvsp: ENST00000520309.1:c.1947A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18497
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11781
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 986
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7673
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1347
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Ser649Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: DP

http://identifiers.org/exac.variant/2-190571713-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571713
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571713
    reference: chr 2
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1252A>C
  hgvsp: ENSP00000407459.1:p.Thr418Pro
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1960A>C
  hgvsp: ENSP00000313513.4:p.Thr654Pro
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1747A>C
  hgvsp: ENSP00000399928.2:p.Thr583Pro
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1960A>C
  hgvsp: ENSP00000427882.1:p.Thr654Pro
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1252A>C
  hgvsp: ENSP00000281412.6:p.Thr418Pro
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1747A>C
  hgvsp: ENSP00000393043.2:p.Thr583Pro
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1960A>C
  hgvsp: ENSP00000397243.2:p.Thr654Pro
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.119A>C
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24734
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18452
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2909
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr654Pro
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: African
population: Other
population: Latino
reference allele: A
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

2-190571717-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571717
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571717
    reference: chr 2
allele count: 1
allele frequency: 8.252050634582693e-6
allele num: 121182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1751T>C
  hgvsp: ENSP00000393043.2:p.Ile584Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1256T>C
  hgvsp: ENSP00000407459.1:p.Ile419Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1964T>C
  hgvsp: ENSP00000397243.2:p.Ile655Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1751T>C
  hgvsp: ENSP00000399928.2:p.Ile584Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1964T>C
  hgvsp: ENSP00000313513.4:p.Ile655Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1256T>C
  hgvsp: ENSP00000281412.6:p.Ile419Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1964T>C
  hgvsp: ENSP00000427882.1:p.Ile655Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.123T>C
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 510
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18450
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24731
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46544
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ile655Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

2-190571727-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571727
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571727
    reference: chr 2
allele count: 23
allele frequency: 1.898566994650994e-4
allele num: 121144
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1974G>A
  hgvsp: ENST00000438402.2:c.1974G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1974G>A
  hgvsp: ENST00000313581.4:c.1974G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1266G>A
  hgvsp: ENST00000441800.1:c.1266G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1266G>A
  hgvsp: ENST00000281412.6:c.1266G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1974G>A
  hgvsp: ENST00000520309.1:c.1974G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1761G>A
  hgvsp: ENST00000433782.2:c.1761G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.133G>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1761G>A
  hgvsp: ENST00000431575.2:c.1761G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24714
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 11789
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 263
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18394
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 9.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 428
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu658Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: FS

http://identifiers.org/exac.variant/2-190571732-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571732
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571732
    reference: chr 2
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1766C>A
  hgvsp: ENSP00000399928.2:p.Ser589Tyr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1979C>A
  hgvsp: ENSP00000397243.2:p.Ser660Tyr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1271C>A
  hgvsp: ENSP00000281412.6:p.Ser424Tyr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.138C>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1271C>A
  hgvsp: ENSP00000407459.1:p.Ser424Tyr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1979C>A
  hgvsp: ENSP00000313513.4:p.Ser660Tyr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1979C>A
  hgvsp: ENSP00000427882.1:p.Ser660Tyr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1766C>A
  hgvsp: ENSP00000393043.2:p.Ser589Tyr
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 24712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46408
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 429
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Ser660Tyr
num of homozygotes: 0
population: Other
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP

2-190571736-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571736
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571736
    reference: chr 2
allele count: 2
allele frequency: 1.65188231990353e-5
allele num: 121074
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1983C>T
  hgvsp: ENST00000438402.2:c.1983C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1983C>T
  hgvsp: ENST00000313581.4:c.1983C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1275C>T
  hgvsp: ENST00000441800.1:c.1275C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1275C>T
  hgvsp: ENST00000281412.6:c.1275C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1770C>T
  hgvsp: ENST00000431575.2:c.1770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.142C>T
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1983C>T
  hgvsp: ENST00000520309.1:c.1983C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1770C>T
  hgvsp: ENST00000433782.2:c.1770C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11790
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18322
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24708
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 168
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7657
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ile661Ile
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

2-190571737-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571737
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571737
    reference: chr 2
allele count: 3
allele frequency: 2.478355693609147e-5
allele num: 121048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.143G>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1276G>A
  hgvsp: ENSP00000281412.6:p.Gly426Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.1984G>A
  hgvsp: ENSP00000397243.2:p.Gly662Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1771G>A
  hgvsp: ENSP00000393043.2:p.Gly591Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1771G>A
  hgvsp: ENSP00000399928.2:p.Gly591Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.1984G>A
  hgvsp: ENSP00000427882.1:p.Gly662Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.1984G>A
  hgvsp: ENSP00000313513.4:p.Gly662Ser
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1276G>A
  hgvsp: ENSP00000407459.1:p.Gly426Ser
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24709
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18289
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2905
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11784
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 985
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7651
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 427
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gly662Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

2-190571762-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571762
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571762
    reference: chr 2
allele count: 1
allele frequency: 8.292011476143882e-6
allele num: 120598
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.2009T>C
  hgvsp: ENSP00000313513.4:p.Ile670Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.168T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1301T>C
  hgvsp: ENSP00000407459.1:p.Ile434Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1796T>C
  hgvsp: ENSP00000393043.2:p.Ile599Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.2009T>C
  hgvsp: ENSP00000427882.1:p.Ile670Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.2009T>C
  hgvsp: ENSP00000397243.2:p.Ile670Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1796T>C
  hgvsp: ENSP00000399928.2:p.Ile599Thr
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1301T>C
  hgvsp: ENSP00000281412.6:p.Ile434Thr
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11746
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2894
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 349
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 262
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ile670Thr
num of homozygotes: 0
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD

2-190571772-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571772
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571772
    reference: chr 2
allele count: 1
allele frequency: 8.319190709127816e-6
allele num: 120204
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1806T>A
  hgvsp: ENSP00000393043.2:p.Asn602Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.2019T>A
  hgvsp: ENSP00000313513.4:p.Asn673Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1806T>A
  hgvsp: ENSP00000399928.2:p.Asn602Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.2019T>A
  hgvsp: ENSP00000397243.2:p.Asn673Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1311T>A
  hgvsp: ENSP00000281412.6:p.Asn437Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.178T>A
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.2019T>A
  hgvsp: ENSP00000427882.1:p.Asn673Lys
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1311T>A
  hgvsp: ENSP00000407459.1:p.Asn437Lys
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24433
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2890
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11734
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 694
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 981
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17602
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 422
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1087
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn673Lys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: South Asian
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

2-190571775-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571775
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571775
    reference: chr 2
allele count: 41
allele frequency: 3.418261855532582e-4
allele num: 119944
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.2022T>C
  hgvsp: ENST00000313581.4:c.2022T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1314T>C
  hgvsp: ENST00000441800.1:c.1314T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.2022T>C
  hgvsp: ENST00000520309.1:c.2022T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.2022T>C
  hgvsp: ENST00000438402.2:c.2022T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1314T>C
  hgvsp: ENST00000281412.6:c.1314T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.181T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1809T>C
  hgvsp: ENST00000433782.2:c.1809T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1809T>C
  hgvsp: ENST00000431575.2:c.1809T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 656
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11721
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 24333
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 946
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2884
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17279
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 5.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 4.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 650
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 417
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1437
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asn674Asn
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: T
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQ

2-190571776-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571776
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571776
    reference: chr 2
allele count: 4960
allele frequency: 4.136228693418727e-2
allele num: 119916
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.2023A>G
  hgvsp: ENSP00000427882.1:p.Ile675Val
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1810A>G
  hgvsp: ENSP00000393043.2:p.Ile604Val
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1810A>G
  hgvsp: ENSP00000399928.2:p.Ile604Val
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.2023A>G
  hgvsp: ENSP00000313513.4:p.Ile675Val
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1315A>G
  hgvsp: ENSP00000281412.6:p.Ile439Val
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.182A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.2023A>G
  hgvsp: ENSP00000397243.2:p.Ile675Val
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1315A>G
  hgvsp: ENSP00000407459.1:p.Ile439Val
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 4.25e1
  variant carriers: 538
genotype depth: GenotypeDepth
  all individuals: 497
  bin: 5.75e1
  variant carriers: 444
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 6.75e1
  variant carriers: 304
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.75e1
  variant carriers: 185
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 9.25e1
  variant carriers: 77
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 368
  bin: 6.25e1
  variant carriers: 320
genotype depth: GenotypeDepth
  all individuals: 23585
  bin: 2.75e1
  variant carriers: 203
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 8.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 2821
  bin: 3.75e1
  variant carriers: 449
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 951
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 428
  bin: 9.75e1
  variant carriers: 337
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 7.25e1
  variant carriers: 229
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 8.25e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 5.25e1
  variant carriers: 478
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 4.75e1
  variant carriers: 561
genotype depth: GenotypeDepth
  all individuals: 11277
  bin: 3.25e1
  variant carriers: 365
genotype depth: GenotypeDepth
  all individuals: 16210
  bin: 2.25e1
  variant carriers: 71
genotype quality: GenotypeQuality
  all individuals: 803
  bin: 7.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1444
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile675Val
num of homozygotes: 133
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: African
population: Latino
reference allele: A
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

2-190571794-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571794
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571794
    reference: chr 2
allele count: 1
allele frequency: 8.6071852782703e-6
allele num: 116182
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1828T>C
  hgvsp: ENST00000431575.2:c.1828T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.2041T>C
  hgvsp: ENST00000313581.4:c.2041T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1333T>C
  hgvsp: ENST00000281412.6:c.1333T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1828T>C
  hgvsp: ENST00000433782.2:c.1828T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1333T>C
  hgvsp: ENST00000441800.1:c.1333T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.200T>C
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.2041T>C
  hgvsp: ENST00000520309.1:c.2041T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.2041T>C
  hgvsp: ENST00000438402.2:c.2041T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2387
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 635
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23364
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 869
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11594
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 438
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7118
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1017
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu681Leu
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: African
reference allele: T
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

2-190571797-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571797
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571797
    reference: chr 2
allele count: 240
allele frequency: 2.095191535426197e-3
allele num: 114548
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.2044A>G
  hgvsp: ENSP00000427882.1:p.Thr682Ala
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1831A>G
  hgvsp: ENSP00000399928.2:p.Thr611Ala
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1336A>G
  hgvsp: ENSP00000281412.6:p.Thr446Ala
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.2044A>G
  hgvsp: ENSP00000397243.2:p.Thr682Ala
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1336A>G
  hgvsp: ENSP00000407459.1:p.Thr446Ala
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.203A>G
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.2044A>G
  hgvsp: ENSP00000313513.4:p.Thr682Ala
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1831A>G
  hgvsp: ENSP00000393043.2:p.Thr611Ala
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11301
  bin: 3.25e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 1.25e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 1.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 13100
  bin: 2.25e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 3151
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 5.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 22175
  bin: 2.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 3.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 684
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 360
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 9.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 214
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr682Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/2-190571797-AC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 190571797
    reference: chr 2
  end: Position
    type: ExactPosition
    position: 190571796
    reference: chr 2
allele count: 1
allele frequency: 8.729964730942487e-6
allele num: 114548
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000399928
  ensembl transcript: ENST00000433782
  gene symbol: ANKAR
  hgvsc: ENST00000433782.2:c.1833delC
  hgvsp: ENSP00000399928.2:p.His613IlefsTer8
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000397243
  ensembl transcript: ENST00000438402
  gene symbol: ANKAR
  hgvsc: ENST00000438402.2:c.2046delC
  hgvsp: ENSP00000397243.2:p.His684IlefsTer8
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000281412
  ensembl transcript: ENST00000281412
  gene symbol: ANKAR
  hgvsc: ENST00000281412.6:c.1338delC
  hgvsp: ENSP00000281412.6:p.His448IlefsTer8
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000407459
  ensembl transcript: ENST00000441800
  gene symbol: ANKAR
  hgvsc: ENST00000441800.1:c.1338delC
  hgvsp: ENSP00000407459.1:p.His448IlefsTer8
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000151687
  ensembl transcript: ENST00000464687
  gene symbol: ANKAR
  hgvsc: ENST00000464687.1:n.205delC
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000393043
  ensembl transcript: ENST00000431575
  gene symbol: ANKAR
  hgvsc: ENST00000431575.2:c.1833delC
  hgvsp: ENSP00000393043.2:p.His613IlefsTer8
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000427882
  ensembl transcript: ENST00000520309
  gene symbol: ANKAR
  hgvsc: ENST00000520309.1:c.2046delC
  hgvsp: ENSP00000427882.1:p.His684IlefsTer8
  variant of: http://identifiers.org/hgnc/26350
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000151687
  ensembl protein: ENSP00000313513
  ensembl transcript: ENST00000313581
  gene symbol: ANKAR
  hgvsc: ENST00000313581.4:c.2046delC
  hgvsp: ENSP00000313513.4:p.His684IlefsTer8
  variant of: http://identifiers.org/hgnc/26350
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3151
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2564
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13100
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5516
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 49
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 271
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1317
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.25e1
  variant carriers: 0
hgvs: p.His684IlefsTer8
num of homozygotes: 0
reference allele: AC

GenotypeQuality
all individuals: 2087
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 679
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31937
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 6
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4260
bin: 7.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 1.984e0

DP
type: SiteQuality
SIO_000300: 2.542536e6

MQRankSum
type: SiteQuality
SIO_000300: 4.3e-1

QD
type: SiteQuality
SIO_000300: 1.241e1

MQ
type: SiteQuality
SIO_000300: 5.925e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -5.056e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.36e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.13e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.55e-1

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

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31938
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2086
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4260
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 2720
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.057e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.841e0

VQSLOD
type: SiteQuality
SIO_000300: 1.85e0

DP
type: SiteQuality
SIO_000300: 2.542454e6

MQRankSum
type: SiteQuality
SIO_000300: 1.1e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.4e-1

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

GenotypeQuality
all individuals: 2086
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3911
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14247
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2720
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 825
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31937
bin: 6.25e1
variant carriers: 0

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

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.21153380179307e-4
allele num: 16508
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.22e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.850000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.6e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.45e-1

FS
type: SiteQuality
SIO_000300: 2.472e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.27e0

MQ
type: SiteQuality
SIO_000300: 5.977e1

QD
type: SiteQuality
SIO_000300: 1.593e1

DP
type: SiteQuality
SIO_000300: 2.542728e6

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 3.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 679
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2087
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3913
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2717
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4260
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 31938
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11536
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.542585e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.861e0

QD
type: SiteQuality
SIO_000300: 1.127e1

MQ
type: SiteQuality
SIO_000300: 5.866e1

MQRankSum
type: SiteQuality
SIO_000300: -2.31e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.895e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.425e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.65e0

FS
type: SiteQuality
SIO_000300: 6.905e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

GenotypeQuality
all individuals: 679
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4260
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3913
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 825
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2716
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 9.79e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.514e0

FS
type: SiteQuality
SIO_000300: 1.4715e1

QD
type: SiteQuality
SIO_000300: 1.567e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.0e-1

DP
type: SiteQuality
SIO_000300: 2.542585e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 5.959e1

VQSLOD
type: SiteQuality
SIO_000300: -2.064e0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.25e1
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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bin: 7.25e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11538
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

QD
type: SiteQuality
SIO_000300: 1.519e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.162e0

FS
type: SiteQuality
SIO_000300: 1.974e0

DP
type: SiteQuality
SIO_000300: 2.542669e6

VQSLOD
type: SiteQuality
SIO_000300: 1.72e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.639999999999999e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.951e0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.665511265164645e-5
allele num: 11540
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 6.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.324e0

DP
type: SiteQuality
SIO_000300: 2.542784e6

QD
type: SiteQuality
SIO_000300: 1.486e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.68e0

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

MQ
type: SiteQuality
SIO_000300: 5.988e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.83e-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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.66e0

MQ
type: SiteQuality
SIO_000300: 5.969e1

FS
type: SiteQuality
SIO_000300: 1.459e0

VQSLOD
type: SiteQuality
SIO_000300: -1.921e-1

QD
type: SiteQuality
SIO_000300: 1.291e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.609e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.42e0

DP
type: SiteQuality
SIO_000300: 2.542706e6

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 2.586e0

MQRankSum
type: SiteQuality
SIO_000300: -3.54e-1

QD
type: SiteQuality
SIO_000300: 1.288e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -6.843e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.279e0

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

DP
type: SiteQuality
SIO_000300: 2.542691e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.87e-1

MQ
type: SiteQuality
SIO_000300: 5.965e1

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 3
allele frequency: 2.600104004160167e-4
allele num: 11538
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 26
allele frequency: 3.895714713814804e-4
allele num: 66740
num of homozygotes: 0

African
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allele count: 9
allele frequency: 8.648856428983279e-4
allele num: 10406
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 2.547121e6

ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.26e-1

MQ
type: SiteQuality
SIO_000300: 5.98e1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -4.9e-2

BaseQRankSum
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SIO_000300: 1.45e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
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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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

African
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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: 0
allele frequency: 0.0e0
allele num: 8654
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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Latino
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allele count: 3
allele frequency: 2.59920291110726e-4
allele num: 11542
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

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

Latino
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allele count: 2
allele frequency: 1.732501732501733e-4
allele num: 11544
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 5.34e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.1e-1

VQSLOD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
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SIO_000300: 1.04e0

ReadPosRankSum
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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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

East Asian
type: Population
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allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

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

African
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.159999999999999e-1

DP
type: SiteQuality
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BaseQRankSum
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4261
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2085
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.939e1

FS
type: SiteQuality
SIO_000300: 1.0104e1

DP
type: SiteQuality
SIO_000300: 2.544026e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 2.82e0

VQSLOD
type: SiteQuality
SIO_000300: -9.401e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.54e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.24e-1

QD
type: SiteQuality
SIO_000300: 1.169e1

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

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3913
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2707
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2082
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 14248
bin: 6.75e1
variant carriers: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498351813005694e-5
allele num: 66740
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.42e-2

FS
type: SiteQuality
SIO_000300: 5.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

QD
type: SiteQuality
SIO_000300: 1.166e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.54e-1

DP
type: SiteQuality
SIO_000300: 2.548753e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

GenotypeQuality
all individuals: 820
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 31967
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 14248
bin: 6.75e1
variant carriers: 0

East Asian
type: Population
allele count: 37
allele frequency: 4.275479547030275e-3
allele num: 8654
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

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

African
type: Population
allele count: 5
allele frequency: 4.804920238324044e-4
allele num: 10406
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.996703626011388e-5
allele num: 66740
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 5.27e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

DP
type: SiteQuality
SIO_000300: 2.548753e6

QD
type: SiteQuality
SIO_000300: 1.166e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.54e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.42e-2

MQ
type: SiteQuality
SIO_000300: 5.968e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.03e-1

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

GenotypeQuality
all individuals: 680
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 2
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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
all individuals: 2662
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variant carriers: 3

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31990
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variant carriers: 0

GenotypeQuality
all individuals: 2081
bin: 8.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

Latino
type: Population
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: 16510
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.134e0

DP
type: SiteQuality
SIO_000300: 2.545095e6

MQRankSum
type: SiteQuality
SIO_000300: 9.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 2.47e0

QD
type: SiteQuality
SIO_000300: 1.041e1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.12e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.0e-2

GenotypeQuality
all individuals: 3917
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 680
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 0
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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: 3
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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: 2660
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variant carriers: 1

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14260
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 0
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variant carriers: 0

GenotypeQuality
all individuals: 820
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66740
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.919e1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.19e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.95e0

FS
type: SiteQuality
SIO_000300: 5.389e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e0

QD
type: SiteQuality
SIO_000300: 9.550000000000001e0

DP
type: SiteQuality
SIO_000300: 2.544936e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.21e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.941e-1

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 820
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variant carriers: 0

GenotypeQuality
all individuals: 0
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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: 2081
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4261
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66738
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 5.817e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.86e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

MQ
type: SiteQuality
SIO_000300: 5.936e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -2.73e-1

DP
type: SiteQuality
SIO_000300: 2.544895e6

QD
type: SiteQuality
SIO_000300: 1.592e1

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 819
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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: 2661
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 19
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 14260
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 681
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 31987
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 3
allele frequency: 2.598302442404296e-4
allele num: 11546
num of homozygotes: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.4983967155144e-5
allele num: 66738
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.825e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.110000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.08e1

MQRankSum
type: SiteQuality
SIO_000300: -4.6e-1

DP
type: SiteQuality
SIO_000300: 2.545205e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.89e-1

FS
type: SiteQuality
SIO_000300: 6.014e0

MQ
type: SiteQuality
SIO_000300: 5.966e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.4e0

GenotypeQuality
all individuals: 22
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 681
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variant carriers: 0

GenotypeQuality
all individuals: 2080
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variant carriers: 0

GenotypeQuality
all individuals: 31989
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
all individuals: 2658
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 4259
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variant carriers: 0

GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 819
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3918
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14262
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498441620714457e-5
allele num: 66736
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

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

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

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

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

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

ClippingRankSum
type: SiteQuality
SIO_000300: -1.869e0

DP
type: SiteQuality
SIO_000300: 2.544967e6

QD
type: SiteQuality
SIO_000300: 1.372e1

MQRankSum
type: SiteQuality
SIO_000300: -7.32e-1

MQ
type: SiteQuality
SIO_000300: 5.895e1

VQSLOD
type: SiteQuality
SIO_000300: -2.386e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.83e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.22e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 1.503e0

GenotypeQuality
all individuals: 1
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 14124
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
all individuals: 2
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variant carriers: 0

GenotypeQuality
all individuals: 0
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
all individuals: 3839
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GenotypeQuality
all individuals: 31774
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variant carriers: 0

GenotypeQuality
all individuals: 4118
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3601
bin: 9.75e1
variant carriers: 2122

European (Finnish)
type: Population
allele count: 144
allele frequency: 2.177199879044451e-2
allele num: 6614
num of homozygotes: 5

African
type: Population
allele count: 38
allele frequency: 3.651739381126273e-3
allele num: 10406
num of homozygotes: 0

South Asian
type: Population
allele count: 119
allele frequency: 7.207752877044215e-3
allele num: 16510
num of homozygotes: 2

Latino
type: Population
allele count: 143
allele frequency: 1.238309664011084e-2
allele num: 11548
num of homozygotes: 1

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

Other
type: Population
allele count: 26
allele frequency: 2.863436123348018e-2
allele num: 908
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1687
allele frequency: 2.527871014145289e-2
allele num: 66736
num of homozygotes: 25

MQ
type: SiteQuality
SIO_000300: 5.966e1

DP
type: SiteQuality
SIO_000300: 2.772146e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.52e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.71e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.974e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.79e-1

QD
type: SiteQuality
SIO_000300: 1.251e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.05e-1

FS
type: SiteQuality
SIO_000300: 5.24e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 614
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2010
bin: 8.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66736
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8654
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.611687812379854e-5
allele num: 10404
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.177e0

DP
type: SiteQuality
SIO_000300: 2.584464e6

MQ
type: SiteQuality
SIO_000300: 5.969e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.32e0

MQRankSum
type: SiteQuality
SIO_000300: 1.51e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.734e0

FS
type: SiteQuality
SIO_000300: 5.98e0

QD
type: SiteQuality
SIO_000300: 1.285e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.34e-1

GenotypeQuality
all individuals: 709
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.056935190793458e-5
allele num: 16510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

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

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

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

VQSLOD
type: SiteQuality
SIO_000300: -3.702e-1

DP
type: SiteQuality
SIO_000300: 2.584377e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.251e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.36e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

MQRankSum
type: SiteQuality
SIO_000300: 1.75e0

FS
type: SiteQuality
SIO_000300: 2.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.297e1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.51e-1

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 2
allele frequency: 1.922337562475971e-4
allele num: 10404
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 8.96e-1

QD
type: SiteQuality
SIO_000300: 1.258e1

DP
type: SiteQuality
SIO_000300: 2.584239e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.13e-1

FS
type: SiteQuality
SIO_000300: 1.887e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.110000000000001e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.113e0

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1538
bin: 9.75e1
variant carriers: 4

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66734
num of homozygotes: 0

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

South Asian
type: Population
allele count: 4
allele frequency: 2.422774076317383e-4
allele num: 16510
num of homozygotes: 0

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.131e0

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.68e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.487e0

FS
type: SiteQuality
SIO_000300: 1.367e0

QD
type: SiteQuality
SIO_000300: 1.06e1

DP
type: SiteQuality
SIO_000300: 2.584542e6

MQ
type: SiteQuality
SIO_000300: 5.965e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.76e-1

GenotypeQuality
all individuals: 32846
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1534
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 3
bin: 3.25e1
variant carriers: 0

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

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

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

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

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.278e0

DP
type: SiteQuality
SIO_000300: 2.58414e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.701e0

MQRankSum
type: SiteQuality
SIO_000300: 1.28e-1

QD
type: SiteQuality
SIO_000300: 1.416e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 5.8e-2

FS
type: SiteQuality
SIO_000300: 5.75e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.2e-2

GenotypeQuality
all individuals: 1
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 2006
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 9.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
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: 16510
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.99e-1

QD
type: SiteQuality
SIO_000300: 1.329e1

VQSLOD
type: SiteQuality
SIO_000300: 1.93e-1

FS
type: SiteQuality
SIO_000300: 2.125e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -8.9e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.99e0

MQ
type: SiteQuality
SIO_000300: 5.951e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.486e0

DP
type: SiteQuality
SIO_000300: 2.584042e6

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32850
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 4.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498621268433042e-5
allele num: 66728
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.421e0

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.72e0

MQRankSum
type: SiteQuality
SIO_000300: 1.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.3e-1

QD
type: SiteQuality
SIO_000300: 1.267e1

MQ
type: SiteQuality
SIO_000300: 5.983e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.584028e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.199999999999999e-2

GenotypeQuality
all individuals: 4
bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2006
bin: 8.25e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.661008141347653e-5
allele num: 11546
num of homozygotes: 0

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

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

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

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

FS
type: SiteQuality
SIO_000300: 5.765e0

ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.003e0

QD
type: SiteQuality
SIO_000300: 1.049e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

MQRankSum
type: SiteQuality
SIO_000300: 9.88e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.584036e6

VQSLOD
type: SiteQuality
SIO_000300: 2.11e-1

GenotypeQuality
all individuals: 32819
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 8

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66724
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

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

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

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

Latino
type: Population
allele count: 8
allele frequency: 6.928806513078123e-4
allele num: 11546
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 6.96e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.19e-1

DP
type: SiteQuality
SIO_000300: 2.584192e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.31e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.597e0

MQRankSum
type: SiteQuality
SIO_000300: 4.89e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.66e0

QD
type: SiteQuality
SIO_000300: 1.281e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQ
type: SiteQuality
SIO_000300: 5.991e1

GenotypeQuality
all individuals: 14629
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
all individuals: 83
bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 7

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 2.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 8.992536194958184e-5
allele num: 66722
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 8.662508662508663e-5
allele num: 11544
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 2.443e0

DP
type: SiteQuality
SIO_000300: 2.584436e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.43e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.23e-1

QD
type: SiteQuality
SIO_000300: 1.258e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.85e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

VQSLOD
type: SiteQuality
SIO_000300: 2.91e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.826e0

GenotypeQuality
all individuals: 709
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 130
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 7
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variant carriers: 0

GenotypeQuality
all individuals: 2005
bin: 8.25e1
variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66720
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.478e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.583053e6

MQRankSum
type: SiteQuality
SIO_000300: 9.15e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 6.32e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.14e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.31e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 5.962e1

GenotypeQuality
all individuals: 5
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14596
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variant carriers: 0

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 2006
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
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variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4297
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.53e0

MQ
type: SiteQuality
SIO_000300: 5.99e1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 7.0e-1

MQRankSum
type: SiteQuality
SIO_000300: 8.75e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

DP
type: SiteQuality
SIO_000300: 2.580568e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.3e-2

QD
type: SiteQuality
SIO_000300: 1.259e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.55e-1

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

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

GenotypeQuality
all individuals: 3985
bin: 7.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2006
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variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 0

GenotypeQuality
all individuals: 1516
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 709
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499115521842113e-5
allele num: 66706
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 5.931e1

VQSLOD
type: SiteQuality
SIO_000300: -2.147e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.64e0

FS
type: SiteQuality
SIO_000300: 3.543e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.33e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.91e-2

DP
type: SiteQuality
SIO_000300: 2.580371e6

QD
type: SiteQuality
SIO_000300: 2.611e1

MQRankSum
type: SiteQuality
SIO_000300: -1.199e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.97e-1

GenotypeQuality
all individuals: 154
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3960
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 25
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variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 117
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 1997
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 9.25e1
variant carriers: 0

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

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

African
type: Population
allele count: 2
allele frequency: 1.963864886095837e-4
allele num: 10184
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66642
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

FS
type: SiteQuality
SIO_000300: 1.917e0

QD
type: SiteQuality
SIO_000300: 8.82e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.7e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQ
type: SiteQuality
SIO_000300: 5.81e1

DP
type: SiteQuality
SIO_000300: 2.576266e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.344e0

MQRankSum
type: SiteQuality
SIO_000300: -2.48e-1

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

GenotypeQuality
all individuals: 62
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variant carriers: 0

GenotypeQuality
all individuals: 244
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GenotypeQuality
all individuals: 9
bin: 4.25e1
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GenotypeQuality
all individuals: 1501
bin: 9.75e1
variant carriers: 3

GenotypeQuality
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GenotypeQuality
all individuals: 1984
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variant carriers: 0

GenotypeQuality
all individuals: 702
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GenotypeQuality
all individuals: 610
bin: 8.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.507753335737469e-5
allele num: 66552
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10080
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16494
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.860000000000001e-1

FS
type: SiteQuality
SIO_000300: 1.271e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.68e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.543e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.4e-3

MQRankSum
type: SiteQuality
SIO_000300: 2.43e-1

MQ
type: SiteQuality
SIO_000300: 5.998e1

VQSLOD
type: SiteQuality
SIO_000300: 3.01e0

QD
type: SiteQuality
SIO_000300: 1.301e1

DP
type: SiteQuality
SIO_000300: 2.578574e6

GenotypeQuality
all individuals: 85
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5184
bin: 3.25e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
all individuals: 3
bin: 5.75e1
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GenotypeQuality
all individuals: 1908
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
all individuals: 9130
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2119
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1398
bin: 9.75e1
variant carriers: 15

East Asian
type: Population
allele count: 15
allele frequency: 1.754796443612541e-3
allele num: 8548
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11388
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9686
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65544
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 5.36e0

VQSLOD
type: SiteQuality
SIO_000300: 4.9e-1

MQ
type: SiteQuality
SIO_000300: 5.994e1

FS
type: SiteQuality
SIO_000300: 2.054e0

MQRankSum
type: SiteQuality
SIO_000300: -3.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.55e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

QD
type: SiteQuality
SIO_000300: 1.611e1

DP
type: SiteQuality
SIO_000300: 2.715879e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.48e-1

GenotypeQuality
all individuals: 440
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 13636
bin: 2.25e1
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GenotypeQuality
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GenotypeQuality
all individuals: 6
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1385
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4534
bin: 6.75e1
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GenotypeQuality
all individuals: 323
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GenotypeQuality
all individuals: 344
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11130
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63234
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.131287297527707e-4
allele num: 9384
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15740
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8296
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6502
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-2

FS
type: SiteQuality
SIO_000300: 3.199e0

QD
type: SiteQuality
SIO_000300: 1.285e1

MQ
type: SiteQuality
SIO_000300: 6.069e1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.572e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.1e-1

DP
type: SiteQuality
SIO_000300: 2.961943e6

VQSLOD
type: SiteQuality
SIO_000300: -5.678e-1

GenotypeQuality
all individuals: 322
bin: 7.5e0
variant carriers: 319

GenotypeQuality
all individuals: 2727
bin: 7.75e1
variant carriers: 2725

GenotypeQuality
all individuals: 23260
bin: 9.75e1
variant carriers: 23259

GenotypeQuality
all individuals: 2863
bin: 6.75e1
variant carriers: 2862

GenotypeQuality
all individuals: 2428
bin: 5.25e1
variant carriers: 2428

GenotypeQuality
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bin: 4.25e1
variant carriers: 2105

GenotypeQuality
all individuals: 796
bin: 2.25e1
variant carriers: 796

GenotypeQuality
all individuals: 2692
bin: 6.25e1
variant carriers: 2690

GenotypeQuality
all individuals: 1575
bin: 3.75e1
variant carriers: 1574

GenotypeQuality
all individuals: 3274
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variant carriers: 3274

GenotypeQuality
all individuals: 2330
bin: 9.25e1
variant carriers: 2330

GenotypeQuality
all individuals: 3393
bin: 7.25e1
variant carriers: 3391

Other
type: Population
allele count: 870
allele frequency: 9.954233409610984e-1
allele num: 874
num of homozygotes: 433

European (Finnish)
type: Population
allele count: 6530
allele frequency: 1.0e0
allele num: 6530
num of homozygotes: 3265

Latino
type: Population
allele count: 11116
allele frequency: 9.964144854786662e-1
allele num: 11156
num of homozygotes: 5538

African
type: Population
allele count: 8888
allele frequency: 9.518098093810238e-1
allele num: 9338
num of homozygotes: 4231

European (Non-Finnish)
type: Population
allele count: 63520
allele frequency: 9.983653967056456e-1
allele num: 63624
num of homozygotes: 31708

South Asian
type: Population
allele count: 15665
allele frequency: 9.980249745158002e-1
allele num: 15696
num of homozygotes: 7817

East Asian
type: Population
allele count: 8175
allele frequency: 9.991444634563676e-1
allele num: 8182
num of homozygotes: 4084

FS
type: SiteQuality
SIO_000300: 2.319e0

MQ
type: SiteQuality
SIO_000300: 6.05e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.45e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

QD
type: SiteQuality
SIO_000300: 2.753e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.5e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

DP
type: SiteQuality
SIO_000300: 1.96783e6

GenotypeQuality
all individuals: 2863
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3102
bin: 5.75e1
variant carriers: 5

GenotypeQuality
all individuals: 2330
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2727
bin: 7.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1575
bin: 3.75e1
variant carriers: 3

GenotypeQuality
all individuals: 23260
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1161
bin: 2.75e1
variant carriers: 13

GenotypeQuality
all individuals: 691
bin: 1.75e1
variant carriers: 20

GenotypeQuality
all individuals: 2349
bin: 4.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3393
bin: 7.25e1
variant carriers: 2

GenotypeQuality
all individuals: 2105
bin: 4.25e1
variant carriers: 8

GenotypeQuality
all individuals: 3143
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 5
allele frequency: 5.354465624330692e-4
allele num: 9338
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 7.171029042667623e-4
allele num: 11156
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 36
allele frequency: 5.658242172764995e-4
allele num: 63624
num of homozygotes: 0

South Asian
type: Population
allele count: 17
allele frequency: 1.083078491335372e-3
allele num: 15696
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.288329519450801e-3
allele num: 874
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.666585186995844e-4
allele num: 8182
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

FS
type: SiteQuality
SIO_000300: 2.319e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

DP
type: SiteQuality
SIO_000300: 1.96783e6

MQ
type: SiteQuality
SIO_000300: 6.05e1

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.45e-2

QD
type: SiteQuality
SIO_000300: 2.753e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

GenotypeQuality
all individuals: 3143
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1411
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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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 796
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2428
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2727
bin: 7.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8182
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9338
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11156
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6530
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.715201810637495e-5
allele num: 63624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15696
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.0e-2

DP
type: SiteQuality
SIO_000300: 1.96783e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.45e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

QD
type: SiteQuality
SIO_000300: 2.753e1

FS
type: SiteQuality
SIO_000300: 2.319e0

ClippingRankSum
type: SiteQuality
SIO_000300: -4.33e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.76e0

BaseQRankSum
type: SiteQuality
SIO_000300: 9.5e-1

MQ
type: SiteQuality
SIO_000300: 6.05e1

GenotypeQuality
all individuals: 614
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40221
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 155
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2385
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variant carriers: 1

GenotypeQuality
all individuals: 1222
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 651
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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
all individuals: 7316
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variant carriers: 0

GenotypeQuality
all individuals: 1322
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 252
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65690
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.790710308298248e-5
allele num: 14726
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: 11456
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10194
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 7.96e-1

DP
type: SiteQuality
SIO_000300: 1.643265e6

FS
type: SiteQuality
SIO_000300: 6.351e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.32e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.78e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.421e0

QD
type: SiteQuality
SIO_000300: 1.411e1

GenotypeQuality
all individuals: 50
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 254
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variant carriers: 0

GenotypeQuality
all individuals: 1406
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variant carriers: 0

GenotypeQuality
all individuals: 1079
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variant carriers: 0

GenotypeQuality
all individuals: 67
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variant carriers: 0

GenotypeQuality
all individuals: 496
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variant carriers: 0

GenotypeQuality
all individuals: 554
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variant carriers: 0

GenotypeQuality
all individuals: 7343
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variant carriers: 0

GenotypeQuality
all individuals: 1173
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 652
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variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14812
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521190179196203e-5
allele num: 65738
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11456
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: 886
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.71e0

DP
type: SiteQuality
SIO_000300: 1.649212e6

QD
type: SiteQuality
SIO_000300: 1.102e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.77e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.1e-3

MQ
type: SiteQuality
SIO_000300: 5.848e1

FS
type: SiteQuality
SIO_000300: 7.277e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.458e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.1e0

VQSLOD
type: SiteQuality
SIO_000300: -4.889e0

GenotypeQuality
all individuals: 645
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7403
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 312
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variant carriers: 0

GenotypeQuality
all individuals: 566
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variant carriers: 0

GenotypeQuality
all individuals: 157
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variant carriers: 0

GenotypeQuality
all individuals: 1172
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variant carriers: 0

GenotypeQuality
all individuals: 326
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GenotypeQuality
all individuals: 2388
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variant carriers: 4

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1318
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.0779189205616e-5
allele num: 65812
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10202
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14962
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 4.05e0

VQSLOD
type: SiteQuality
SIO_000300: 4.34e0

QD
type: SiteQuality
SIO_000300: 1.509e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.9e-3

DP
type: SiteQuality
SIO_000300: 1.658974e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 3.68e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.7e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.04e-1

GenotypeQuality
all individuals: 2389
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 42844
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variant carriers: 0

GenotypeQuality
all individuals: 260
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variant carriers: 0

GenotypeQuality
all individuals: 515
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variant carriers: 0

GenotypeQuality
all individuals: 1304
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 247
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variant carriers: 0

GenotypeQuality
all individuals: 857
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1313
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variant carriers: 0

GenotypeQuality
all individuals: 138
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15008
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.556915879332868e-5
allele num: 65834
num of homozygotes: 0

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

African
type: Population
allele count: 2
allele frequency: 1.958863858961802e-4
allele num: 10210
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 1
allele frequency: 1.158211721102618e-4
allele num: 8634
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.406e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.74e-1

FS
type: SiteQuality
SIO_000300: 4.533e0

DP
type: SiteQuality
SIO_000300: 1.666822e6

MQRankSum
type: SiteQuality
SIO_000300: 1.32e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.28e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

QD
type: SiteQuality
SIO_000300: 1.116e1

GenotypeQuality
all individuals: 98
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44322
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variant carriers: 0

GenotypeQuality
all individuals: 471
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 323
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 106
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variant carriers: 0

GenotypeQuality
all individuals: 667
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GenotypeQuality
all individuals: 1181
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 426
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 315
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 259
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.771350400625366e-5
allele num: 10234
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.029201502483945e-5
allele num: 66024
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11468
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15346
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 9.02e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.17e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

FS
type: SiteQuality
SIO_000300: 1.274e0

DP
type: SiteQuality
SIO_000300: 1.680765e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.2e-2

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.96e0

QD
type: SiteQuality
SIO_000300: 1.387e1

GenotypeQuality
all individuals: 79
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1334
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 819
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variant carriers: 0

GenotypeQuality
all individuals: 9
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GenotypeQuality
all individuals: 262
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variant carriers: 0

GenotypeQuality
all individuals: 428
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GenotypeQuality
all individuals: 2383
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
all individuals: 75
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GenotypeQuality
all individuals: 143
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GenotypeQuality
all individuals: 1195
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variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 5.75e1
variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11478
num of homozygotes: 0

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: 15686
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10260
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.511030522816561e-5
allele num: 66180
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 7.32e-1

FS
type: SiteQuality
SIO_000300: 4.176e0

MQ
type: SiteQuality
SIO_000300: 5.967e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.06e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.699999999999999e-3

QD
type: SiteQuality
SIO_000300: 1.486e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.88e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.32e0

MQRankSum
type: SiteQuality
SIO_000300: 6.24e-1

DP
type: SiteQuality
SIO_000300: 1.690466e6

GenotypeQuality
all individuals: 241
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 94
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variant carriers: 0

GenotypeQuality
all individuals: 264
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variant carriers: 0

GenotypeQuality
all individuals: 45134
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variant carriers: 0

GenotypeQuality
all individuals: 752
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variant carriers: 0

GenotypeQuality
all individuals: 32
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variant carriers: 0

GenotypeQuality
all individuals: 10
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GenotypeQuality
all individuals: 426
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GenotypeQuality
all individuals: 7550
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variant carriers: 0

GenotypeQuality
all individuals: 131
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GenotypeQuality
all individuals: 2382
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1195
bin: 7.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 2
allele frequency: 1.948178453146308e-4
allele num: 10266
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15760
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11480
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66214
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.33e0

VQSLOD
type: SiteQuality
SIO_000300: 1.48e0

MQRankSum
type: SiteQuality
SIO_000300: 6.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 1.69245e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.339e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.63e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

QD
type: SiteQuality
SIO_000300: 1.311e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 8.75e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 9

GenotypeQuality
all individuals: 689
bin: 2.25e1
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GenotypeQuality
all individuals: 67
bin: 4.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

South Asian
type: Population
allele count: 9
allele frequency: 5.685407454200885e-4
allele num: 15830
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10272
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: 0
allele frequency: 0.0e0
allele num: 66250
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.05e-1

QD
type: SiteQuality
SIO_000300: 1.538e1

MQRankSum
type: SiteQuality
SIO_000300: 5.83e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.06e-1

DP
type: SiteQuality
SIO_000300: 1.694299e6

FS
type: SiteQuality
SIO_000300: 4.475e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.02e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.21e-1

GenotypeQuality
all individuals: 2382
bin: 9.75e1
variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 45576
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66326
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.232859636000998e-5
allele num: 16044
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10280
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 896
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.061e1

DP
type: SiteQuality
SIO_000300: 1.698662e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.58e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.28e-1

FS
type: SiteQuality
SIO_000300: 1.207e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

QD
type: SiteQuality
SIO_000300: 9.09e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -6.76e-1

GenotypeQuality
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bin: 7.5e0
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: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507658907248824e-5
allele num: 66328
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11494
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16084
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 5.74e-1

FS
type: SiteQuality
SIO_000300: 4.745e0

DP
type: SiteQuality
SIO_000300: 1.699271e6

MQRankSum
type: SiteQuality
SIO_000300: 1.09e0

MQ
type: SiteQuality
SIO_000300: 5.947e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.6e-2

QD
type: SiteQuality
SIO_000300: 1.201e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.019e0

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
all individuals: 1211
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GenotypeQuality
all individuals: 670
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.697164724299878e-5
allele num: 11498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66488
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16336
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.95e-1

QD
type: SiteQuality
SIO_000300: 1.37e1

MQRankSum
type: SiteQuality
SIO_000300: -2.042e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.16e-2

DP
type: SiteQuality
SIO_000300: 1.705628e6

FS
type: SiteQuality
SIO_000300: 7.16e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.436e0

MQ
type: SiteQuality
SIO_000300: 5.974e1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.063545961678389e-5
allele num: 16492
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66614
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.473e1

DP
type: SiteQuality
SIO_000300: 1.710864e6

MQRankSum
type: SiteQuality
SIO_000300: -6.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.59e-1

FS
type: SiteQuality
SIO_000300: 1.1952e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.43e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.19e-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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bin: 6.25e1
variant carriers: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

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

South Asian
type: Population
allele count: 8
allele frequency: 4.849072614862408e-4
allele num: 16498
num of homozygotes: 1

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-2

BaseQRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: -3.07e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.69e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.941e1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: -8.4e-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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bin: 7.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10336
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
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allele num: 906
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.6253e1

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.375e0

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.711454e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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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: 45

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 8652
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000570108320581e-5
allele num: 66654
num of homozygotes: 0

Other
type: Population
allele count: 0
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allele num: 906
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.689607229753215e-5
allele num: 11508
num of homozygotes: 0

African
type: Population
allele count: 42
allele frequency: 4.063467492260062e-3
allele num: 10336
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.714006e6

BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.165e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.27e-2

MQ
type: SiteQuality
SIO_000300: 5.96e1

MQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.64e-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
all individuals: 10
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GenotypeQuality
all individuals: 23
bin: 5.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10332
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000210014701029e-5
allele num: 66662
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 8.399999999999999e-3

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.182e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.213e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.62e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

DP
type: SiteQuality
SIO_000300: 1.711402e6

GenotypeQuality
all individuals: 12
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 3.75e1
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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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bin: 4.75e1
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
all individuals: 2340
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 17
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66668
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 1.1968e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.53e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.799999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: 4.14e-1

MQ
type: SiteQuality
SIO_000300: 5.953e1

QD
type: SiteQuality
SIO_000300: 9.27e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.51e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.062e0

DP
type: SiteQuality
SIO_000300: 1.711373e6

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

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 671
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variant carriers: 0

GenotypeQuality
all individuals: 429
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499970000599988e-5
allele num: 66668
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10322
num of homozygotes: 0

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

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

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.42e-1

MQ
type: SiteQuality
SIO_000300: 5.972e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.88e-1

VQSLOD
type: SiteQuality
SIO_000300: -5.999999999999999e-4

FS
type: SiteQuality
SIO_000300: 8.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.394e0

QD
type: SiteQuality
SIO_000300: 1.37e1

DP
type: SiteQuality
SIO_000300: 1.711381e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.7e0

GenotypeQuality
all individuals: 14
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 669
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variant carriers: 0

GenotypeQuality
all individuals: 2354
bin: 9.75e1
variant carriers: 23

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.500990217847926e-5
allele num: 66652
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10300
num of homozygotes: 0

Latino
type: Population
allele count: 20
allele frequency: 1.737317581653926e-3
allele num: 11512
num of homozygotes: 0

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

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

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

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

DP
type: SiteQuality
SIO_000300: 1.711685e6

BaseQRankSum
type: SiteQuality
SIO_000300: -2.649e0

MQRankSum
type: SiteQuality
SIO_000300: 3.88e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.67e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.14e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

FS
type: SiteQuality
SIO_000300: 5.39e-1

GenotypeQuality
all individuals: 4
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 3.75e1
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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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1208
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variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66628
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11510
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16504
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.15e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.41e-1

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.92e-1

QD
type: SiteQuality
SIO_000300: 1.016e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.744e0

MQ
type: SiteQuality
SIO_000300: 5.978e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-3

FS
type: SiteQuality
SIO_000300: 2.8e0

DP
type: SiteQuality
SIO_000300: 1.709835e6

GenotypeQuality
all individuals: 46386
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 1
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GenotypeQuality
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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: 4
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2333
bin: 9.75e1
variant carriers: 2

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66618
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

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

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21197430614471e-4
allele num: 16502
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.04e-1

QD
type: SiteQuality
SIO_000300: 1.275e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -9.350000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 1.79e0

DP
type: SiteQuality
SIO_000300: 1.709483e6

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.95e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 25
bin: 3.75e1
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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variant carriers: 3

GenotypeQuality
all individuals: 30
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002822653294096e-5
allele num: 66604
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11508
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.61e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.02e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.2e-3

MQ
type: SiteQuality
SIO_000300: 5.948e1

FS
type: SiteQuality
SIO_000300: 4.707e0

QD
type: SiteQuality
SIO_000300: 1.288e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.87e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.64e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.9e-1

DP
type: SiteQuality
SIO_000300: 1.709231e6

GenotypeQuality
all individuals: 659
bin: 2.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 9.844457570387872e-5
allele num: 10158
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16462
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66362
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -6.55e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.92e-1

DP
type: SiteQuality
SIO_000300: 1.701112e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.47e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.18e-1

MQ
type: SiteQuality
SIO_000300: 5.925e1

VQSLOD
type: SiteQuality
SIO_000300: 4.04e-1

QD
type: SiteQuality
SIO_000300: 1.451e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 80
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GenotypeQuality
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GenotypeQuality
all individuals: 38
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 262
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GenotypeQuality
all individuals: 656
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GenotypeQuality
all individuals: 1318
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variant carriers: 0

GenotypeQuality
all individuals: 7549
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66122
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10116
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11440
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.090133982947625e-5
allele num: 16420
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -4.71e-1

QD
type: SiteQuality
SIO_000300: 1.008e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.884e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.11e-1

VQSLOD
type: SiteQuality
SIO_000300: -7.069e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.89e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.77e-1

DP
type: SiteQuality
SIO_000300: 1.694631e6

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 73
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GenotypeQuality
all individuals: 117
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GenotypeQuality
all individuals: 1317
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2348
bin: 9.75e1
variant carriers: 41

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7514
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44861
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 118
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16394
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 32
allele frequency: 4.852455038971279e-4
allele num: 65946
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 2.217294900221729e-3
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10092
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.06544901065449e-3
allele num: 6570
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.733e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.71e0

MQRankSum
type: SiteQuality
SIO_000300: -6.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.76e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.5e0

DP
type: SiteQuality
SIO_000300: 1.689988e6

MQ
type: SiteQuality
SIO_000300: 5.959e1

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 4.75e1
variant carriers: 2

GenotypeQuality
all individuals: 99
bin: 9.25e1
variant carriers: 6

GenotypeQuality
all individuals: 84
bin: 8.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 17
bin: 1.75e1
variant carriers: 2

GenotypeQuality
all individuals: 7075
bin: 6.75e1
variant carriers: 2

GenotypeQuality
all individuals: 43909
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1054
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 269
bin: 8.25e1
variant carriers: 7

GenotypeQuality
all individuals: 5352
bin: 9.75e1
variant carriers: 4803

GenotypeQuality
all individuals: 86
bin: 5.25e1
variant carriers: 1

South Asian
type: Population
allele count: 1125
allele frequency: 6.86226668293278e-2
allele num: 16394
num of homozygotes: 46

European (Non-Finnish)
type: Population
allele count: 2985
allele frequency: 4.52766654532217e-2
allele num: 65928
num of homozygotes: 71

East Asian
type: Population
allele count: 201
allele frequency: 2.335579828026958e-2
allele num: 8606
num of homozygotes: 3

European (Finnish)
type: Population
allele count: 296
allele frequency: 4.503956177723676e-2
allele num: 6572
num of homozygotes: 7

Other
type: Population
allele count: 34
allele frequency: 3.76940133037694e-2
allele num: 902
num of homozygotes: 1

African
type: Population
allele count: 175
allele frequency: 1.734046769718589e-2
allele num: 10092
num of homozygotes: 3

Latino
type: Population
allele count: 144
allele frequency: 1.260724916827176e-2
allele num: 11422
num of homozygotes: 2

FS
type: SiteQuality
SIO_000300: 7.47e-1

QD
type: SiteQuality
SIO_000300: 1.608e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.26e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e0

MQRankSum
type: SiteQuality
SIO_000300: 6.5e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.34e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.49e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.66e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

DP
type: SiteQuality
SIO_000300: 1.782072e6

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

GenotypeQuality
all individuals: 42745
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6422
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 213
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 76
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 289
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 748
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 5.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.576441655894315e-5
allele num: 63434
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16094
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11100
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: 0
allele frequency: 0.0e0
allele num: 8428
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9780
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.03e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.28e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 4.61e0

MQ
type: SiteQuality
SIO_000300: 5.998e1

MQRankSum
type: SiteQuality
SIO_000300: 4.84e-1

QD
type: SiteQuality
SIO_000300: 1.542e1

FS
type: SiteQuality
SIO_000300: 4.587e0

DP
type: SiteQuality
SIO_000300: 1.562519e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.21e0

GenotypeQuality
all individuals: 121
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40352
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 949
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 580
bin: 2.75e1
variant carriers: 1

GenotypeQuality
all individuals: 233
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 355
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8675
bin: 2.25e1
variant carriers: 1

GenotypeQuality
all individuals: 729
bin: 9.75e1
variant carriers: 239

GenotypeQuality
all individuals: 6622
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 8.25e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6410
num of homozygotes: 0

Latino
type: Population
allele count: 20
allele frequency: 1.829491401390413e-3
allele num: 10932
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15968
num of homozygotes: 0

African
type: Population
allele count: 193
allele frequency: 1.995863495346432e-2
allele num: 9670
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8368
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 27
allele frequency: 4.332338500048137e-4
allele num: 62322
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.526217e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.53e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.11e-1

QD
type: SiteQuality
SIO_000300: 1.52e1

FS
type: SiteQuality
SIO_000300: 9.26e-1

MQRankSum
type: SiteQuality
SIO_000300: 2.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.63e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.35e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-2