16-67208155-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208155
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208155
    reference: chr 16
allele count: 1
allele frequency: 9.821060281668008e-6
allele num: 101822
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.83G>A
  hgvsp: ENSP00000454598.1:p.Gly28Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.269G>A
  hgvsp: ENSP00000457243.1:p.Gly90Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.83G>A
  hgvsp: ENSP00000268605.7:p.Gly28Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.83G>A
  hgvsp: ENSP00000457720.1:p.Gly28Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.83G>A
  hgvsp: ENSP00000454256.1:p.Gly28Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.83G>A
  hgvsp: ENSP00000399831.2:p.Gly28Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.83G>A
  hgvsp: ENSP00000457732.1:p.Gly28Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.187G>A
  hgvsp: ENSP00000455808.1:p.Gly63Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+206G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.184G>A
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27712
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2973
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1883
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1290
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12766
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7237
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1214
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3184
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Gly28Glu
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
reference allele: G
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS

16-67208167-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208167
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208167
    reference: chr 16
allele count: 4
allele frequency: 4.131719208362599e-5
allele num: 96812
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.95A>G
  hgvsp: ENSP00000454256.1:p.Asp32Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.281A>G
  hgvsp: ENSP00000457243.1:p.Asp94Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.196A>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.95A>G
  hgvsp: ENSP00000457720.1:p.Asp32Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.95A>G
  hgvsp: ENSP00000457732.1:p.Asp32Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.95A>G
  hgvsp: ENSP00000268605.7:p.Asp32Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.199A>G
  hgvsp: ENSP00000455808.1:p.Asp67Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.95A>G
  hgvsp: ENSP00000399831.2:p.Asp32Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.95A>G
  hgvsp: ENSP00000454598.1:p.Asp32Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+218A>G
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11533
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9638
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1185
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2027
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3657
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2813
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 356
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Asp32Gly
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-67208168-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208168
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208168
    reference: chr 16
allele count: 2
allele frequency: 2.080905610121525e-5
allele num: 96112
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.96C>A
  hgvsp: ENSP00000454598.1:p.Asp32Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.200C>A
  hgvsp: ENSP00000455808.1:p.Asp67Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.96C>A
  hgvsp: ENSP00000457720.1:p.Asp32Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.197C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+219C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.96C>A
  hgvsp: ENSP00000399831.2:p.Asp32Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.96C>A
  hgvsp: ENSP00000454256.1:p.Asp32Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.282C>A
  hgvsp: ENSP00000457243.1:p.Asp94Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.96C>A
  hgvsp: ENSP00000457732.1:p.Asp32Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.96C>A
  hgvsp: ENSP00000268605.7:p.Asp32Glu
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9893
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11375
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2761
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Asp32Glu
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

16-67208168-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208168
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208168
    reference: chr 16
allele count: 2
allele frequency: 2.080905610121525e-5
allele num: 96112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.96C>T
  hgvsp: ENST00000563439.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.96C>T
  hgvsp: ENST00000432069.2:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.96C>T
  hgvsp: ENST00000564992.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+219C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.282C>T
  hgvsp: ENST00000564053.1:c.282C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.96C>T
  hgvsp: ENST00000568146.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.200C>T
  hgvsp: ENST00000566871.1:c.200C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.197C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.96C>T
  hgvsp: ENST00000268605.7:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.96C>T
  hgvsp: ENST00000565560.1:c.96C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11375
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1221
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3771
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23398
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9893
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8384
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14969
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Asp32Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

16-67208172-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208172
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208172
    reference: chr 16
allele count: 1
allele frequency: 1.060580349567283e-5
allele num: 94288
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.100C>T
  hgvsp: ENST00000432069.2:c.100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.100C>T
  hgvsp: ENST00000268605.7:c.100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.286C>T
  hgvsp: ENST00000564053.1:c.286C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.201C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.100C>T
  hgvsp: ENST00000564992.1:c.100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.100C>T
  hgvsp: ENST00000565560.1:c.100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.100C>T
  hgvsp: ENST00000568146.1:c.100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+223C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.100C>T
  hgvsp: ENST00000563439.1:c.100C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.204C>T
  hgvsp: ENST00000566871.1:c.204C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8970
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22439
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10830
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2120
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Leu34Leu
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum

http://identifiers.org/exac.variant/16-67208179-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208179
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208179
    reference: chr 16
allele count: 1
allele frequency: 1.108819550706318e-5
allele num: 90186
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.293C>A
  hgvsp: ENSP00000457243.1:p.Ala98Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+230C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.107C>A
  hgvsp: ENSP00000399831.2:p.Ala36Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.107C>A
  hgvsp: ENSP00000454598.1:p.Ala36Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.107C>A
  hgvsp: ENSP00000457720.1:p.Ala36Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.107C>A
  hgvsp: ENSP00000457732.1:p.Ala36Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.107C>A
  hgvsp: ENSP00000268605.7:p.Ala36Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.107C>A
  hgvsp: ENSP00000454256.1:p.Ala36Glu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.208C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.211C>A
  hgvsp: ENSP00000455808.1:p.Ala71Glu
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2216
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9493
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4192
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20160
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 993
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ala36Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

16-67208181-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208181
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208181
    reference: chr 16
allele count: 6
allele frequency: 6.718774495532015e-5
allele num: 89302
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.109C>T
  hgvsp: ENSP00000457720.1:p.Arg37Trp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+232C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.109C>T
  hgvsp: ENSP00000454598.1:p.Arg37Trp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.109C>T
  hgvsp: ENSP00000457732.1:p.Arg37Trp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.109C>T
  hgvsp: ENSP00000454256.1:p.Arg37Trp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.295C>T
  hgvsp: ENSP00000457243.1:p.Arg99Trp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.109C>T
  hgvsp: ENSP00000399831.2:p.Arg37Trp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.109C>T
  hgvsp: ENSP00000268605.7:p.Arg37Trp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.210C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.213C>T
  hgvsp: ENSP00000455808.1:p.Arg72Trp
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2239
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 45
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 19806
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4142
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13100
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9235
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1016
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 317
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2195
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg37Trp
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ

16-67208182-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208182
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208182
    reference: chr 16
allele count: 1
allele frequency: 1.124606387764283e-5
allele num: 88920
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.110G>A
  hgvsp: ENSP00000457732.1:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.110G>A
  hgvsp: ENSP00000457720.1:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.110G>A
  hgvsp: ENSP00000399831.2:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.110G>A
  hgvsp: ENSP00000454598.1:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+233G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.211G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.296G>A
  hgvsp: ENSP00000457243.1:p.Arg99Gln
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.110G>A
  hgvsp: ENSP00000454256.1:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.110G>A
  hgvsp: ENSP00000268605.7:p.Arg37Gln
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.214G>A
  hgvsp: ENSP00000455808.1:p.Arg72Gln
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10753
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2180
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg37Gln
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: QD

16-67208182-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208182
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208182
    reference: chr 16
allele count: 1
allele frequency: 1.124606387764283e-5
allele num: 88920
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.110G>C
  hgvsp: ENSP00000399831.2:p.Arg37Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.110G>C
  hgvsp: ENSP00000454598.1:p.Arg37Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.110G>C
  hgvsp: ENSP00000268605.7:p.Arg37Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.110G>C
  hgvsp: ENSP00000457720.1:p.Arg37Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.214G>C
  hgvsp: ENSP00000455808.1:p.Arg72Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.110G>C
  hgvsp: ENSP00000454256.1:p.Arg37Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.296G>C
  hgvsp: ENSP00000457243.1:p.Arg99Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.211G>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+233G>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.110G>C
  hgvsp: ENSP00000457732.1:p.Arg37Pro
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13269
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9186
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10753
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4048
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19701
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 473
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 613
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg37Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: QD

16-67208190-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208190
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208190
    reference: chr 16
allele count: 1
allele frequency: 1.187112704480163e-5
allele num: 84238
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.118C>T
  hgvsp: ENSP00000268605.7:p.Leu40Phe
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.118C>T
  hgvsp: ENSP00000457720.1:p.Leu40Phe
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.118C>T
  hgvsp: ENSP00000454256.1:p.Leu40Phe
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+241C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.219C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.118C>T
  hgvsp: ENSP00000457732.1:p.Leu40Phe
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.118C>T
  hgvsp: ENSP00000454598.1:p.Leu40Phe
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.118C>T
  hgvsp: ENSP00000399831.2:p.Leu40Phe
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.222C>T
  hgvsp: ENSP00000455808.1:p.Leu75Phe
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.304C>T
  hgvsp: ENSP00000457243.1:p.Leu102Phe
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7679
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17145
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2393
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15521
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4196
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12448
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 840
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 649
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 735
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Leu40Phe
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: ClippingRankSum

16-67208194-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208194
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208194
    reference: chr 16
allele count: 10
allele frequency: 1.212768021732803e-4
allele num: 82456
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.226C>T
  hgvsp: ENSP00000455808.1:p.Thr76Ile
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.122C>T
  hgvsp: ENSP00000268605.7:p.Thr41Ile
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.308C>T
  hgvsp: ENSP00000457243.1:p.Thr103Ile
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.122C>T
  hgvsp: ENSP00000457720.1:p.Thr41Ile
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.122C>T
  hgvsp: ENSP00000454256.1:p.Thr41Ile
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+245C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.122C>T
  hgvsp: ENSP00000399831.2:p.Thr41Ile
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.122C>T
  hgvsp: ENSP00000454598.1:p.Thr41Ile
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.223C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.122C>T
  hgvsp: ENSP00000457732.1:p.Thr41Ile
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4080
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12861
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7347
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16322
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1717
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 177
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr41Ile
num of homozygotes: 1
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: DP

16-67208195-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208195
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208195
    reference: chr 16
allele count: 2
allele frequency: 2.450559952949249e-5
allele num: 81614
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+246C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.123C>T
  hgvsp: ENST00000568146.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.309C>T
  hgvsp: ENST00000564053.1:c.309C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.123C>T
  hgvsp: ENST00000565560.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.123C>T
  hgvsp: ENST00000563439.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.123C>T
  hgvsp: ENST00000268605.7:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.123C>T
  hgvsp: ENST00000432069.2:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.224C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.123C>T
  hgvsp: ENST00000564992.1:c.123C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.227C>T
  hgvsp: ENST00000566871.1:c.227C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13016
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4056
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7239
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2522
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 202
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr41Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum

16-67208195-CG-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208195
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208194
    reference: chr 16
allele count: 3
allele frequency: 3.675839929423874e-5
allele num: 81614
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.227delG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.230delG
  hgvsp: ENSP00000455808.1:p.Pro78GlnfsTer22
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.126delG
  hgvsp: ENSP00000457732.1:p.Pro43GlnfsTer?
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.126delG
  hgvsp: ENSP00000454256.1:p.Pro43GlnfsTer?
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.126delG
  hgvsp: ENSP00000268605.7:p.Pro43GlnfsTer181
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.312delG
  hgvsp: ENSP00000457243.1:p.Pro105GlnfsTer181
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.126delG
  hgvsp: ENSP00000454598.1:p.Pro43GlnfsTer60
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.126delG
  hgvsp: ENSP00000457720.1:p.Pro43GlnfsTer?
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+249delG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.126delG
  hgvsp: ENSP00000399831.2:p.Pro43GlnfsTer181
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7239
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16560
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4056
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2477
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 830
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13016
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2473
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2522
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Pro43GlnfsTer60
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
reference allele: CG
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ

16-67208196-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208196
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208196
    reference: chr 16
allele count: 1
allele frequency: 1.236919575489202e-5
allele num: 80846
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.124G>C
  hgvsp: ENSP00000268605.7:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.124G>C
  hgvsp: ENSP00000399831.2:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+247G>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.124G>C
  hgvsp: ENSP00000454598.1:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.124G>C
  hgvsp: ENSP00000454256.1:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.124G>C
  hgvsp: ENSP00000457732.1:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.124G>C
  hgvsp: ENSP00000457720.1:p.Gly42Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.228G>C
  hgvsp: ENSP00000455808.1:p.Gly77Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.225G>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.310G>C
  hgvsp: ENSP00000457243.1:p.Gly104Arg
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 13208
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3926
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16883
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7124
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19473
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2532
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Gly42Arg
num of homozygotes: 0
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff

16-67208197-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208197
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208197
    reference: chr 16
allele count: 1
allele frequency: 1.242297753925661e-5
allele num: 80496
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.125G>T
  hgvsp: ENSP00000457732.1:p.Gly42Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.125G>T
  hgvsp: ENSP00000399831.2:p.Gly42Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.311G>T
  hgvsp: ENSP00000457243.1:p.Gly104Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.229G>T
  hgvsp: ENSP00000455808.1:p.Gly77Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.125G>T
  hgvsp: ENSP00000268605.7:p.Gly42Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.125G>T
  hgvsp: ENSP00000457720.1:p.Gly42Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.226G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.125G>T
  hgvsp: ENSP00000454256.1:p.Gly42Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+248G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.125G>T
  hgvsp: ENSP00000454598.1:p.Gly42Val
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2565
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13390
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17206
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 759
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6966
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15547
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 545
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly42Val
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

16-67208199-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208199
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208199
    reference: chr 16
allele count: 1
allele frequency: 1.267619916844133e-5
allele num: 78888
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.228C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.127C>T
  hgvsp: ENSP00000454598.1:p.Pro43Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.127C>T
  hgvsp: ENSP00000399831.2:p.Pro43Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.127C>T
  hgvsp: ENSP00000457720.1:p.Pro43Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.127C>T
  hgvsp: ENSP00000454256.1:p.Pro43Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.127C>T
  hgvsp: ENSP00000268605.7:p.Pro43Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.231C>T
  hgvsp: ENSP00000455808.1:p.Pro78Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.313C>T
  hgvsp: ENSP00000457243.1:p.Pro105Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.127C>T
  hgvsp: ENSP00000457732.1:p.Pro43Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+250C>T
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17825
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13728
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3649
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2626
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14963
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26318
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Pro43Ser
num of homozygotes: 0
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

16-67208204-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208204
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208204
    reference: chr 16
allele count: 1
allele frequency: 1.302727912248248e-5
allele num: 76762
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.233G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+255G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.132G>A
  hgvsp: ENST00000568146.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.132G>A
  hgvsp: ENST00000564992.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.236G>A
  hgvsp: ENST00000566871.1:c.236G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.132G>A
  hgvsp: ENST00000432069.2:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.132G>A
  hgvsp: ENST00000565560.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.132G>A
  hgvsp: ENST00000268605.7:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.318G>A
  hgvsp: ENST00000564053.1:c.318G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.132G>A
  hgvsp: ENST00000563439.1:c.132G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14025
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18850
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 690
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6226
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14296
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 226
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu44Glu
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: Other
population: African
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum

16-67208214-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208214
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208214
    reference: chr 16
allele count: 1
allele frequency: 1.404691670178396e-5
allele num: 71190
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.328T>C
  hgvsp: ENST00000564053.1:c.328T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.142T>C
  hgvsp: ENST00000565560.1:c.142T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.142T>C
  hgvsp: ENST00000268605.7:c.142T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.142T>C
  hgvsp: ENST00000432069.2:c.142T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+265T>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.142T>C
  hgvsp: ENST00000563439.1:c.142T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.142T>C
  hgvsp: ENST00000568146.1:c.142T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.246T>C
  hgvsp: ENST00000566871.1:c.246T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.142T>C
  hgvsp: ENST00000564992.1:c.142T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.243T>C
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 612
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5144
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20898
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15666
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2993
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3511
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Leu48Leu
num of homozygotes: 0
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: BaseQRankSum

16-67208221-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208221
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208221
    reference: chr 16
allele count: 1
allele frequency: 1.491646778042959e-5
allele num: 67040
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.149C>T
  hgvsp: ENSP00000457720.1:p.Ala50Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.149C>T
  hgvsp: ENSP00000268605.7:p.Ala50Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.250C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.149C>T
  hgvsp: ENSP00000399831.2:p.Ala50Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.335C>T
  hgvsp: ENSP00000457243.1:p.Ala112Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.149C>T
  hgvsp: ENSP00000454598.1:p.Ala50Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.149C>T
  hgvsp: ENSP00000457732.1:p.Ala50Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.253C>T
  hgvsp: ENSP00000455808.1:p.Ala85Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+272C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.149C>T
  hgvsp: ENSP00000454256.1:p.Ala50Val
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4564
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16418
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21997
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2915
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4231
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 351
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12464
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala50Val
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD

16-67208223-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208223
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208223
    reference: chr 16
allele count: 1
allele frequency: 1.543495709081929e-5
allele num: 64788
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.151C>T
  hgvsp: ENST00000563439.1:c.151C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+274C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.151C>T
  hgvsp: ENST00000432069.2:c.151C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.151C>T
  hgvsp: ENST00000268605.7:c.151C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.252C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.151C>T
  hgvsp: ENST00000565560.1:c.151C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.151C>T
  hgvsp: ENST00000568146.1:c.151C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.151C>T
  hgvsp: ENST00000564992.1:c.151C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.337C>T
  hgvsp: ENST00000564053.1:c.337C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.255C>T
  hgvsp: ENST00000566871.1:c.255C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 571
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2994
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8315
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16715
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4189
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1262
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1331
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Leu51Leu
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

16-67208231-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208231
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208231
    reference: chr 16
allele count: 2
allele frequency: 3.34851326011251e-5
allele num: 59728
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.345T>C
  hgvsp: ENST00000564053.1:c.345T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.159T>C
  hgvsp: ENST00000565560.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+282T>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.159T>C
  hgvsp: ENST00000268605.7:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.159T>C
  hgvsp: ENST00000568146.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.263T>C
  hgvsp: ENST00000566871.1:c.263T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.159T>C
  hgvsp: ENST00000564992.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.260T>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.159T>C
  hgvsp: ENST00000563439.1:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.159T>C
  hgvsp: ENST00000432069.2:c.159T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2681
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3435
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23826
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16629
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6884
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2843
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Asp53Asp
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum

16-67208235-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208235
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208235
    reference: chr 16
allele count: 4
allele frequency: 7.168972686214065e-5
allele num: 55796
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.163G>A
  hgvsp: ENSP00000457720.1:p.Glu55Lys
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.264G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.163G>A
  hgvsp: ENSP00000268605.7:p.Glu55Lys
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.163G>A
  hgvsp: ENSP00000454598.1:p.Glu55Lys
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.163G>A
  hgvsp: ENSP00000457732.1:p.Glu55Lys
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.163G>A
  hgvsp: ENSP00000399831.2:p.Glu55Lys
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.267G>A
  hgvsp: ENSP00000455808.1:p.Glu90Lys
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.163G>A
  hgvsp: ENSP00000454256.1:p.Glu55Lys
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.63+286G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.349G>A
  hgvsp: ENSP00000457243.1:p.Glu117Lys
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6239
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 465
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16374
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2327
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6789
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24574
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1587
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Glu55Lys
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD

16-67208238-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208238
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208238
    reference: chr 16
allele count: 1
allele frequency: 1.91270418117134e-5
allele num: 52282
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.166C>G
  hgvsp: ENSP00000268605.7:p.Arg56Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.166C>G
  hgvsp: ENSP00000454598.1:p.Arg56Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.352C>G
  hgvsp: ENSP00000457243.1:p.Arg118Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.166C>G
  hgvsp: ENSP00000457720.1:p.Arg56Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-286C>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.166C>G
  hgvsp: ENSP00000454256.1:p.Arg56Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.166C>G
  hgvsp: ENSP00000457732.1:p.Arg56Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.166C>G
  hgvsp: ENSP00000399831.2:p.Arg56Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.267C>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.270C>G
  hgvsp: ENSP00000455808.1:p.Arg91Gly
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5551
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7842
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2273
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2741
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15824
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31876
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2750
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg56Gly
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum

16-67208254-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208254
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208254
    reference: chr 16
allele count: 2
allele frequency: 4.647920055775041e-5
allele num: 43030
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.182T>C
  hgvsp: ENSP00000268605.7:p.Leu61Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.182T>C
  hgvsp: ENSP00000454256.1:p.Leu61Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.283T>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.182T>C
  hgvsp: ENSP00000399831.2:p.Leu61Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.182T>C
  hgvsp: ENSP00000457720.1:p.Leu61Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.368T>C
  hgvsp: ENSP00000457243.1:p.Leu123Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.182T>C
  hgvsp: ENSP00000454598.1:p.Leu61Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-270T>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+11T>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.182T>C
  hgvsp: ENSP00000457732.1:p.Leu61Pro
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4672
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2199
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1401
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26611
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10991
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 537
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 9.75e1
  variant carriers: 2
hgvs: p.Leu61Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: T
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD

16-67208257-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208257
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208257
    reference: chr 16
allele count: 69
allele frequency: 1.69599842690001e-3
allele num: 40684
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.185T>C
  hgvsp: ENSP00000268605.7:p.Leu62Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.286T>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.185T>C
  hgvsp: ENSP00000454598.1:p.Leu62Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-267T>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+14T>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.185T>C
  hgvsp: ENSP00000399831.2:p.Leu62Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.185T>C
  hgvsp: ENSP00000457732.1:p.Leu62Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.185T>C
  hgvsp: ENSP00000457720.1:p.Leu62Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.371T>C
  hgvsp: ENSP00000457243.1:p.Leu124Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.185T>C
  hgvsp: ENSP00000454256.1:p.Leu62Pro
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 12551
  bin: 1.25e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 2079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26515
  bin: 7.5e0
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1366
  bin: 1.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 4425
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11951
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29336
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12240
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Leu62Pro
num of homozygotes: 0
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

16-67208259-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208259
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208259
    reference: chr 16
allele count: 1
allele frequency: 2.476718842876956e-5
allele num: 40376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.187C>T
  hgvsp: ENST00000432069.2:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-265C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.187C>T
  hgvsp: ENST00000565560.1:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.187C>T
  hgvsp: ENST00000563439.1:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.288C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.187C>T
  hgvsp: ENST00000568146.1:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.187C>T
  hgvsp: ENST00000564992.1:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.187C>T
  hgvsp: ENST00000268605.7:c.187C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.373C>T
  hgvsp: ENST00000564053.1:c.373C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+16C>T
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1250
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12016
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26688
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12416
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4460
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 358
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1950
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu63Leu
num of homozygotes: 0
population: European (Finnish)
population: Other
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: MQRankSum

16-67208260-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208260
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208260
    reference: chr 16
allele count: 2
allele frequency: 4.974629390110437e-5
allele num: 40204
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-264T>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.188T>C
  hgvsp: ENSP00000454256.1:p.Leu63Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.188T>C
  hgvsp: ENSP00000399831.2:p.Leu63Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.188T>C
  hgvsp: ENSP00000268605.7:p.Leu63Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.374T>C
  hgvsp: ENSP00000457243.1:p.Leu125Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.188T>C
  hgvsp: ENSP00000457720.1:p.Leu63Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.289T>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.188T>C
  hgvsp: ENSP00000454598.1:p.Leu63Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+17T>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.188T>C
  hgvsp: ENSP00000457732.1:p.Leu63Pro
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4418
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26680
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2076
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1971
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Leu63Pro
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: African
population: European (Non-Finnish)
reference allele: T
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD

16-67208278-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208278
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208278
    reference: chr 16
allele count: 1
allele frequency: 3.3889114816321e-5
allele num: 29508
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.206G>A
  hgvsp: ENSP00000457732.1:p.Gly69Asp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.206G>A
  hgvsp: ENSP00000399831.2:p.Gly69Asp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+35G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.206G>A
  hgvsp: ENSP00000454256.1:p.Gly69Asp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.307G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.206G>A
  hgvsp: ENSP00000268605.7:p.Gly69Asp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.206G>A
  hgvsp: ENSP00000457720.1:p.Gly69Asp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-246G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.392G>A
  hgvsp: ENSP00000457243.1:p.Gly131Asp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.206G>A
  hgvsp: ENSP00000454598.1:p.Gly69Asp
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3220
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9178
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 968
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26483
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16503
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1572
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly69Asp
num of homozygotes: 0
population: Other
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP

16-67208279-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208279
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208279
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 28926
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.308C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.207C>T
  hgvsp: ENST00000268605.7:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+36C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.207C>T
  hgvsp: ENST00000568146.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.207C>T
  hgvsp: ENST00000432069.2:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.207C>T
  hgvsp: ENST00000565560.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.207C>T
  hgvsp: ENST00000564992.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.393C>T
  hgvsp: ENST00000564053.1:c.393C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.207C>T
  hgvsp: ENST00000563439.1:c.207C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-245C>T
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: synonymous
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 982
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26516
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3151
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16651
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9036
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1539
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4257
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1491
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly69Gly
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ

16-67208283-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208283
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208283
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 26964
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.211G>A
  hgvsp: ENSP00000454598.1:p.Ala71Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.211G>A
  hgvsp: ENSP00000268605.7:p.Ala71Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.211G>A
  hgvsp: ENSP00000454256.1:p.Ala71Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.211G>A
  hgvsp: ENSP00000399831.2:p.Ala71Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.397G>A
  hgvsp: ENSP00000457243.1:p.Ala133Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+40G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.312G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.211G>A
  hgvsp: ENSP00000457732.1:p.Ala71Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.211G>A
  hgvsp: ENSP00000457720.1:p.Ala71Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-241G>A
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 944
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26773
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8389
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1419
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17327
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2934
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4081
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala71Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: G
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQ
site quality: FS

16-67208292-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208292
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208292
    reference: chr 16
allele count: 1
allele frequency: 4.120313143798929e-5
allele num: 24270
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.220C>T
  hgvsp: ENSP00000268605.7:p.Gln74Ter
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+49C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.220C>T
  hgvsp: ENSP00000399831.2:p.Gln74Ter
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-232C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.220C>T
  hgvsp: ENSP00000457720.1:p.Gln74Ter
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.220C>T
  hgvsp: ENSP00000457732.1:p.Gln74Ter
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.220C>T
  hgvsp: ENSP00000454256.1:p.Gln74Ter
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.220C>T
  hgvsp: ENSP00000454598.1:p.Gln74Ter
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.406C>T
  hgvsp: ENSP00000457243.1:p.Gln136Ter
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.321C>T
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2294
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27189
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7944
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18301
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 875
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1086
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gln74Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
reference allele: C
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

16-67208310-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208310
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208310
    reference: chr 16
allele count: 8
allele frequency: 3.998400639744102e-4
allele num: 20008
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.238G>A
  hgvsp: ENSP00000268605.7:p.Ala80Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.339G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-214G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.238G>A
  hgvsp: ENSP00000399831.2:p.Ala80Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.238G>A
  hgvsp: ENSP00000454598.1:p.Ala80Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+67G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.238G>A
  hgvsp: ENSP00000454256.1:p.Ala80Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.238G>A
  hgvsp: ENSP00000457720.1:p.Ala80Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.424G>A
  hgvsp: ENSP00000457243.1:p.Ala142Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.238G>A
  hgvsp: ENSP00000457732.1:p.Ala80Thr
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1130
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27553
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 19575
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7646
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 890
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ala80Thr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP

16-67208315-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208315
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208315
    reference: chr 16
allele count: 2
allele frequency: 1.097333479644464e-4
allele num: 18226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.243G>A
  hgvsp: ENST00000268605.7:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+72G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-209G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.243G>A
  hgvsp: ENST00000432069.2:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.243G>A
  hgvsp: ENST00000568146.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.243G>A
  hgvsp: ENST00000565560.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.243G>A
  hgvsp: ENST00000563439.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.243G>A
  hgvsp: ENST00000564992.1:c.243G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.429G>A
  hgvsp: ENST00000564053.1:c.429G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.344G>A
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20304
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19905
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24423
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Gln81Gln
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ

16-67208315-G-GC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208315
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208316
    reference: chr 16
allele count: 1
allele frequency: 5.48666739822232e-5
allele num: 18226
alternate allele: GC
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.244dupC
  hgvsp: ENSP00000399831.2:p.Arg82ProfsTer25
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.244dupC
  hgvsp: ENSP00000268605.7:p.Arg82ProfsTer25
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.244dupC
  hgvsp: ENSP00000457720.1:p.Arg82ProfsTer25
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.244dupC
  hgvsp: ENSP00000454598.1:p.Arg82ProfsTer125
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.244dupC
  hgvsp: ENSP00000457732.1:p.Arg82ProfsTer25
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.345dupC
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+73dupC
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.430dupC
  hgvsp: ENSP00000457243.1:p.Arg144ProfsTer25
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.244dupC
  hgvsp: ENSP00000454256.1:p.Arg82ProfsTer25
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-208dupC
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7475
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20304
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 866
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 718
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27295
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24423
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg82ProfsTer125
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Finnish)
reference allele: G
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/16-67208316-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208316
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208316
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 18092
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.244C>A
  hgvsp: ENSP00000457720.1:p.Arg82Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.244C>A
  hgvsp: ENSP00000457732.1:p.Arg82Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.244C>A
  hgvsp: ENSP00000454598.1:p.Arg82Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.430C>A
  hgvsp: ENSP00000457243.1:p.Arg144Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-208C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+73C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.244C>A
  hgvsp: ENSP00000268605.7:p.Arg82Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.244C>A
  hgvsp: ENSP00000399831.2:p.Arg82Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.244C>A
  hgvsp: ENSP00000454256.1:p.Arg82Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.345C>A
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27361
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20286
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7458
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 712
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 862
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1278
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg82Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

16-67208322-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208322
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208322
    reference: chr 16
allele count: 7
allele frequency: 4.235749727701803e-4
allele num: 16526
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.250G>A
  hgvsp: ENSP00000457732.1:p.Ala84Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-202G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.250G>A
  hgvsp: ENSP00000268605.7:p.Ala84Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.250G>A
  hgvsp: ENSP00000399831.2:p.Ala84Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.250G>A
  hgvsp: ENSP00000454598.1:p.Ala84Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.250G>A
  hgvsp: ENSP00000457720.1:p.Ala84Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.250G>A
  hgvsp: ENSP00000454256.1:p.Ala84Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.436G>A
  hgvsp: ENSP00000457243.1:p.Ala146Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+79G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.351G>A
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27317
  bin: 7.5e0
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7115
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 20864
  bin: 2.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 778
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 195
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3399
  bin: 1.25e1
  variant carriers: 1
hgvs: p.Ala84Thr
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

16-67208329-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208329
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208329
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 13948
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.257C>T
  hgvsp: ENSP00000457732.1:p.Ala86Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.443C>T
  hgvsp: ENSP00000457243.1:p.Ala148Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.257C>T
  hgvsp: ENSP00000457720.1:p.Ala86Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+86C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.257C>T
  hgvsp: ENSP00000268605.7:p.Ala86Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.257C>T
  hgvsp: ENSP00000454598.1:p.Ala86Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.257C>T
  hgvsp: ENSP00000399831.2:p.Ala86Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-195C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.358C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.257C>T
  hgvsp: ENSP00000454256.1:p.Ala86Val
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27179
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 640
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21767
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 244
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala86Val
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

16-67208340-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208340
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208340
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 12654
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.268G>T
  hgvsp: ENSP00000268605.7:p.Ala90Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.268G>T
  hgvsp: ENSP00000457720.1:p.Ala90Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.268G>T
  hgvsp: ENSP00000399831.2:p.Ala90Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.369G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.268G>T
  hgvsp: ENSP00000457732.1:p.Ala90Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.454G>T
  hgvsp: ENSP00000457243.1:p.Ala152Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.268G>T
  hgvsp: ENSP00000454598.1:p.Ala90Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.268G>T
  hgvsp: ENSP00000454256.1:p.Ala90Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-184G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+97G>T
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 5783
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27935
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21771
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala90Ser
num of homozygotes: 0
population: Other
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum

16-67208349-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208349
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208349
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 11722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.378T>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.277T>G
  hgvsp: ENSP00000457732.1:p.Trp93Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.463T>G
  hgvsp: ENSP00000457243.1:p.Trp155Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.277T>G
  hgvsp: ENSP00000454256.1:p.Trp93Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.277T>G
  hgvsp: ENSP00000457720.1:p.Trp93Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.277T>G
  hgvsp: ENSP00000268605.7:p.Trp93Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-175T>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.277T>G
  hgvsp: ENSP00000399831.2:p.Trp93Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+106T>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.277T>G
  hgvsp: ENSP00000454598.1:p.Trp93Gly
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5325
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27725
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21998
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21431
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Trp93Gly
num of homozygotes: 0
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: QD

16-67208361-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208361
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208361
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 11280
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.390G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.289G>A
  hgvsp: ENSP00000454256.1:p.Gly97Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.475G>A
  hgvsp: ENSP00000457243.1:p.Gly159Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.289G>A
  hgvsp: ENSP00000457720.1:p.Gly97Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-163G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.285+4G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.289G>A
  hgvsp: ENSP00000457732.1:p.Gly97Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+118G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.289G>A
  hgvsp: ENSP00000399831.2:p.Gly97Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.289G>A
  hgvsp: ENSP00000268605.7:p.Gly97Ser
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22152
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27456
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1368
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gly97Ser
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/16-67208373-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208373
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208373
    reference: chr 16
allele count: 1
allele frequency: 9.363295880149813e-5
allele num: 10680
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.295+6C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.295+6C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.481+6C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.295+6C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.402C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+130C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.295+6C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-151C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.295+6C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.285+16C>A
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 496
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21946
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4802
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27097
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3401
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 972
  bin: 3.25e1
  variant carriers: 0
hgvs: c.295+6C>A
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff

http://identifiers.org/exac.variant/16-67208377-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208377
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208377
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 10778
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.295+10C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.295+10C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.295+10C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.285+20C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.481+10C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.295+10C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.406C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.295+10C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-147C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.275+134C>A
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21890
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 502
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27115
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 51
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4820
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2145
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 299
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 279
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP

16-67208388-CTA-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208388
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208386
    reference: chr 16
allele count: 1
allele frequency: 8.614748449345279e-5
allele num: 11608
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-135_276-134delTA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-135_64-134delTA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.418_419delTA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.295+22_295+23delTA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.285+32_285+33delTA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.295+22_295+23delTA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.295+22_295+23delTA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.295+22_295+23delTA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.481+22_481+23delTA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.295+22_295+23delTA
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4994
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27795
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21390
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 563
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1553
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: CTA
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD

16-67208393-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208393
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208393
    reference: chr 16
allele count: 0
allele frequency: 0.0e0
allele num: 12008
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.285+36G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-131G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.295+26G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-131G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.295+26G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.295+26G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.422G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.295+26G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.295+26G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.481+26G>A
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 410
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28121
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 602
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5096
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20974
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19843
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1623
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1213
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3294
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

16-67208415-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208415
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208415
    reference: chr 16
allele count: 16
allele frequency: 1.09484056384289e-3
allele num: 14614
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.444G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-109G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.295+48G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.295+48G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.481+48G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-109G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.295+48G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.285+58G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.295+48G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.295+48G>A
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17955
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30273
  bin: 7.5e0
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 948
  bin: 1.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 6147
  bin: 1.25e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1903
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 311
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16464
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2215
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

16-67208479-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208479
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208479
    reference: chr 16
allele count: 4
allele frequency: 4.518446558073334e-5
allele num: 88526
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.508G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.296-45G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.296-45G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.482-45G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.286-45G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.296-45G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.296-45G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.296-45G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-45G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-45G>A
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6082
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14134
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13190
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12060
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13635
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7201
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP

16-67208479-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208479
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208479
    reference: chr 16
allele count: 1
allele frequency: 1.129611639518334e-5
allele num: 88526
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-45G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.296-45G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-45G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.296-45G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.508G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.296-45G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.286-45G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.482-45G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.296-45G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.296-45G>T
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14134
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6082
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12060
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13190
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2423
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 439
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13635
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Other
population: African
population: Latino
population: East Asian
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-67208479-GCA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208479
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208477
    reference: chr 16
allele count: 7
allele frequency: 7.907281476628335e-5
allele num: 88526
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.296-42_296-41delCA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-42_276-41delCA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.482-42_482-41delCA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-42_64-41delCA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.296-42_296-41delCA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.296-42_296-41delCA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.511_512delCA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.296-42_296-41delCA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.286-42_286-41delCA
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.296-42_296-41delCA
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7171
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5028
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12060
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6082
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 817
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13190
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14134
  bin: 1.25e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 1159
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2069
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1693
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: GCA
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

16-67208482-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208482
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208482
    reference: chr 16
allele count: 3
allele frequency: 3.328377748685291e-5
allele num: 90134
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.296-42C>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-42C>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.296-42C>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.511C>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.482-42C>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.296-42C>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.296-42C>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.286-42C>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-42C>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.296-42C>G
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 777
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15788
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7178
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6042
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9641
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13844
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5230
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2648
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4698
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1151
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3345
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum

16-67208483-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208483
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208484
    reference: chr 16
allele count: 1
allele frequency: 1.107885932064435e-5
allele num: 90262
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.296-37dupG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.482-37dupG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.296-37dupG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.296-37dupG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.516dupG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.286-37dupG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.296-37dupG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-37dupG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.296-37dupG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-37dupG
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5324
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7184
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8813
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6029
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13639
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1082
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 389
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18267
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: Other
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: QD

16-67208485-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208485
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208485
    reference: chr 16
allele count: 1
allele frequency: 1.10751783103708e-5
allele num: 90292
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.296-39G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.296-39G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-39G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.296-39G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.482-39G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.514G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.296-39G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.296-39G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-39G>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.286-39G>T
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5999
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13224
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7176
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 814
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7754
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18027
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1062
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19747
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: South Asian
population: African
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP

16-67208494-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208494
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208494
    reference: chr 16
allele count: 1
allele frequency: 1.095410231131559e-5
allele num: 91290
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-30G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.523G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.296-30G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.286-30G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.296-30G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-30G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.482-30G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.296-30G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.296-30G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.296-30G>A
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6733
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7032
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10327
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5832
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3813
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5023
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1100
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 388
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

16-67208503-T-TC
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208503
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208504
    reference: chr 16
allele count: 95
allele frequency: 1.018002571795971e-3
allele num: 93320
alternate allele: TC
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.296-20dupC
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.296-20dupC
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.286-20dupC
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-20dupC
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-20dupC
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.533dupC
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.296-20dupC
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.296-20dupC
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.296-20dupC
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.482-20dupC
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1036
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6638
  bin: 7.5e0
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1982
  bin: 1.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 8051
  bin: 2.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6743
  bin: 1.25e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 5631
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 28804
  bin: 2.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 514
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4980
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 515
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 542
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

16-67208505-A-AGTCG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208505
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208509
    reference: chr 16
allele count: 95
allele frequency: 1.01660816710898e-3
allele num: 93448
alternate allele: AGTCG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.296-19_296-18insGTCG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.286-19_286-18insGTCG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-19_276-18insGTCG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.534_535insGTCG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-19_64-18insGTCG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.296-19_296-18insGTCG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.296-19_296-18insGTCG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.482-19_482-18insGTCG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.296-19_296-18insGTCG
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.296-19_296-18insGTCG
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6603
  bin: 7.5e0
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6136
  bin: 1.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 1.75e1
  variant carriers: 29
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8282
  bin: 2.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29537
  bin: 2.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 445
  bin: 7.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 8.25e1
  variant carriers: 7
genotype quality: GenotypeQuality
  all individuals: 486
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3157
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum

16-67208505-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208505
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208505
    reference: chr 16
allele count: 1
allele frequency: 1.070113860114716e-5
allele num: 93448
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.534A>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.296-19A>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.296-19A>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-19A>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.482-19A>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.296-19A>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.286-19A>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-19A>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.296-19A>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.296-19A>G
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 5548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1795
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29537
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6136
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8282
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6603
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1047
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 33153
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2428
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4996
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-67208506-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208506
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208506
    reference: chr 16
allele count: 1
allele frequency: 1.068125013351563e-5
allele num: 93622
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.296-18C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.482-18C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.535C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.286-18C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.296-18C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.296-18C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-18C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.296-18C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-18C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.296-18C>T
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5910
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6573
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29843
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8391
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5517
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1058
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 462
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 565
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 136
  bin: 8.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/16-67208509-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208509
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208509
    reference: chr 16
allele count: 1
allele frequency: 1.059838480615554e-5
allele num: 94354
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.296-15C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.538C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.296-15C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.482-15C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.296-15C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.286-15C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.276-15C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.296-15C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.296-15C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.64-15C>A
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8834
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5395
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5149
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6477
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1428
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1124
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30616
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1990
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1594
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 8.75e1
  variant carriers: 1
num of homozygotes: 0
population: Latino
population: Other
population: African
population: South Asian
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/16-67208525-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208525
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208525
    reference: chr 16
allele count: 2
allele frequency: 2.058078989071601e-5
allele num: 97178
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.297C>A
  hgvsp: ENST00000564992.1:c.297C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.297C>A
  hgvsp: ENST00000563439.1:c.297C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.277C>A
  hgvsp: ENSP00000455808.1:p.Ala93Asp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.287C>A
  hgvsp: ENSP00000454598.1:p.Ala96Asp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.297C>A
  hgvsp: ENST00000268605.7:c.297C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.65C>A
  hgvsp: ENST00000563258.1:c.65C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.483C>A
  hgvsp: ENST00000564053.1:c.483C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.297C>A
  hgvsp: ENST00000565560.1:c.297C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.297C>A
  hgvsp: ENST00000432069.2:c.297C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.554C>A
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2874
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 843
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4544
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10323
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33160
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala96Asp
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: VQSLOD

16-67208536-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208536
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208536
    reference: chr 16
allele count: 2
allele frequency: 2.031776992157341e-5
allele num: 98436
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.308G>A
  hgvsp: ENSP00000399831.2:p.Arg103His
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.308G>A
  hgvsp: ENSP00000268605.7:p.Arg103His
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.494G>A
  hgvsp: ENSP00000457243.1:p.Arg165His
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.565G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.308G>A
  hgvsp: ENSP00000454256.1:p.Arg103His
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.308G>A
  hgvsp: ENSP00000457720.1:p.Arg103His
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.298G>A
  hgvsp: ENSP00000454598.1:p.Ala100Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.76G>A
  hgvsp: ENSP00000463698.1:p.Arg26His
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.288G>A
  hgvsp: ENSP00000455808.1:p.Ala97Thr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.308G>A
  hgvsp: ENSP00000457732.1:p.Arg103His
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11049
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6567
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33404
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 864
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala100Thr
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD

16-67208555-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208555
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208555
    reference: chr 16
allele count: 1
allele frequency: 1.003009027081244e-5
allele num: 99700
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.327C>T
  hgvsp: ENST00000564992.1:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.513C>T
  hgvsp: ENST00000564053.1:c.513C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.327C>T
  hgvsp: ENST00000563439.1:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.327C>T
  hgvsp: ENST00000432069.2:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.95C>T
  hgvsp: ENST00000563258.1:c.95C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.317C>T
  hgvsp: ENSP00000454598.1:p.Ala106Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.327C>T
  hgvsp: ENST00000268605.7:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.584C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.307C>T
  hgvsp: ENSP00000455808.1:p.Ala103Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.327C>T
  hgvsp: ENST00000565560.1:c.327C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32652
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2504
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12022
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2758
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 900
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7341
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1497
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2397
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala106Val
num of homozygotes: 0
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum

16-67208559-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208559
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208559
    reference: chr 16
allele count: 31
allele frequency: 3.100992317541613e-4
allele num: 99968
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.331G>A
  hgvsp: ENSP00000457732.1:p.Gly111Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.517G>A
  hgvsp: ENSP00000457243.1:p.Gly173Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.588G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.99G>A
  hgvsp: ENSP00000463698.1:p.Gly34Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.331G>A
  hgvsp: ENSP00000399831.2:p.Gly111Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.331G>A
  hgvsp: ENSP00000268605.7:p.Gly111Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.311G>A
  hgvsp: ENST00000566871.1:c.311G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.331G>A
  hgvsp: ENSP00000457720.1:p.Gly111Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.331G>A
  hgvsp: ENSP00000454256.1:p.Gly111Ser
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.321G>A
  hgvsp: ENST00000568146.1:c.321G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7502
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 988
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1443
  bin: 3.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12203
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2319
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32259
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 4.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 2972
  bin: 1.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 806
  bin: 3.25e1
  variant carriers: 1
hgvs: p.Gly34Ser
num of homozygotes: 0
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ

http://identifiers.org/exac.variant/16-67208561-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208561
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208561
    reference: chr 16
allele count: 2
allele frequency: 2.006944026331105e-5
allele num: 99654
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.590C>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.323C>A
  hgvsp: ENSP00000454598.1:p.Ala108Asp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.333C>A
  hgvsp: ENST00000564992.1:c.333C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.333C>A
  hgvsp: ENST00000563439.1:c.333C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.333C>A
  hgvsp: ENST00000268605.7:c.333C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.101C>A
  hgvsp: ENST00000563258.1:c.101C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.519C>A
  hgvsp: ENST00000564053.1:c.519C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.313C>A
  hgvsp: ENSP00000455808.1:p.Ala105Asp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.333C>A
  hgvsp: ENST00000432069.2:c.333C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.333C>A
  hgvsp: ENST00000565560.1:c.333C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7591
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1212
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 31506
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12281
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1472
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8489
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ala108Asp
num of homozygotes: 0
population: African
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: MQ
site quality: QD

16-67208562-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208562
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208562
    reference: chr 16
allele count: 1
allele frequency: 1.001582500350554e-5
allele num: 99842
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.324C>T
  hgvsp: ENST00000568146.1:c.324C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.334C>T
  hgvsp: ENSP00000457720.1:p.His112Tyr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.334C>T
  hgvsp: ENSP00000454256.1:p.His112Tyr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.334C>T
  hgvsp: ENSP00000457732.1:p.His112Tyr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.102C>T
  hgvsp: ENSP00000463698.1:p.His35Tyr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.314C>T
  hgvsp: ENST00000566871.1:c.314C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.520C>T
  hgvsp: ENSP00000457243.1:p.His174Tyr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.591C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.334C>T
  hgvsp: ENSP00000399831.2:p.His112Tyr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.334C>T
  hgvsp: ENSP00000268605.7:p.His112Tyr
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7600
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2212
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3351
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12324
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31536
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8597
  bin: 2.25e1
  variant carriers: 0
hgvs: p.His35Tyr
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum

16-67208566-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208566
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208566
    reference: chr 16
allele count: 1
allele frequency: 1.003290793803676e-5
allele num: 99672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.595G>A
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.338G>A
  hgvsp: ENSP00000457720.1:p.Trp113Ter
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.338G>A
  hgvsp: ENSP00000268605.7:p.Trp113Ter
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.338G>A
  hgvsp: ENSP00000457732.1:p.Trp113Ter
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.524G>A
  hgvsp: ENSP00000457243.1:p.Trp175Ter
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.106G>A
  hgvsp: ENSP00000463698.1:p.Trp36Ter
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.338G>A
  hgvsp: ENSP00000399831.2:p.Trp113Ter
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.318G>A
  hgvsp: ENSP00000455808.1:p.Gly107Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.328G>A
  hgvsp: ENSP00000454598.1:p.Gly110Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.338G>A
  hgvsp: ENSP00000454256.1:p.Trp113Ter
  variant of: http://identifiers.org/hgnc/7869
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 30883
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1455
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7842
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12251
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Trp36Ter
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum

16-67208569-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208569
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208569
    reference: chr 16
allele count: 1
allele frequency: 1.002948669087116e-5
allele num: 99706
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.341C>G
  hgvsp: ENSP00000454256.1:p.Thr114Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.341C>G
  hgvsp: ENSP00000457720.1:p.Thr114Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.598C>G
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.527C>G
  hgvsp: ENSP00000457243.1:p.Thr176Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.109C>G
  hgvsp: ENSP00000463698.1:p.Thr37Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.341C>G
  hgvsp: ENSP00000399831.2:p.Thr114Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.331C>G
  hgvsp: ENSP00000454598.1:p.Arg111Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.321C>G
  hgvsp: ENSP00000455808.1:p.Arg108Gly
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.341C>G
  hgvsp: ENSP00000268605.7:p.Thr114Arg
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.341C>G
  hgvsp: ENSP00000457732.1:p.Thr114Arg
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12301
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 143
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Arg111Gly
num of homozygotes: 0
population: Other
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
reference allele: C
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

16-67208569-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208569
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208569
    reference: chr 16
allele count: 1
allele frequency: 1.002948669087116e-5
allele num: 99706
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.321C>T
  hgvsp: ENSP00000455808.1:p.Arg108Cys
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.341C>T
  hgvsp: ENSP00000399831.2:p.Thr114Met
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.341C>T
  hgvsp: ENSP00000454256.1:p.Thr114Met
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.341C>T
  hgvsp: ENSP00000457732.1:p.Thr114Met
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.109C>T
  hgvsp: ENSP00000463698.1:p.Thr37Met
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.341C>T
  hgvsp: ENSP00000457720.1:p.Thr114Met
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.598C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.341C>T
  hgvsp: ENSP00000268605.7:p.Thr114Met
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.527C>T
  hgvsp: ENSP00000457243.1:p.Thr176Met
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.331C>T
  hgvsp: ENSP00000454598.1:p.Arg111Cys
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3861
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12301
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 30710
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1996
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1461
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7875
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 274
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg111Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

16-67208570-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208570
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208570
    reference: chr 16
allele count: 64
allele frequency: 6.408459166099251e-4
allele num: 99868
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.342G>C
  hgvsp: ENST00000563439.1:c.342G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.332G>C
  hgvsp: ENSP00000454598.1:p.Arg111Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.342G>C
  hgvsp: ENST00000564992.1:c.342G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.342G>C
  hgvsp: ENST00000268605.7:c.342G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.528G>C
  hgvsp: ENST00000564053.1:c.528G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.110G>C
  hgvsp: ENST00000563258.1:c.110G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.322G>C
  hgvsp: ENSP00000455808.1:p.Arg108Pro
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.342G>C
  hgvsp: ENST00000565560.1:c.342G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.599G>C
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.342G>C
  hgvsp: ENST00000432069.2:c.342G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1448
  bin: 3.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 3.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 7903
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12307
  bin: 2.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 4.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1948
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3966
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 5.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30594
  bin: 2.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg111Pro
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
reference allele: G
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum

16-67208572-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208572
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208572
    reference: chr 16
allele count: 1
allele frequency: 1.005955255110253e-5
allele num: 99408
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.344C>T
  hgvsp: ENSP00000457732.1:p.Pro115Leu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.344C>T
  hgvsp: ENSP00000457720.1:p.Pro115Leu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.601C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.530C>T
  hgvsp: ENSP00000457243.1:p.Pro177Leu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.344C>T
  hgvsp: ENSP00000454256.1:p.Pro115Leu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.344C>T
  hgvsp: ENSP00000268605.7:p.Pro115Leu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.112C>T
  hgvsp: ENSP00000463698.1:p.Pro38Leu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.334C>T
  hgvsp: ENSP00000454598.1:p.Arg112Trp
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.344C>T
  hgvsp: ENSP00000399831.2:p.Pro115Leu
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.324C>T
  hgvsp: ENSP00000455808.1:p.Arg109Trp
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1855
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1904
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12243
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4422
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8090
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1444
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36118
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg112Trp
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: C
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: VQSLOD

16-67208578-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 67208578
    reference: chr 16
  end: Position
    type: ExactPosition
    position: 67208578
    reference: chr 16
allele count: 7
allele frequency: 7.037580680835662e-5
allele num: 99466
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454256
  ensembl transcript: ENST00000563439
  gene symbol: NOL3
  hgvsc: ENST00000563439.1:c.350C>T
  hgvsp: ENSP00000454256.1:p.Ala117Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000140939
  ensembl transcript: ENST00000568503
  gene symbol: NOL3
  hgvsc: ENST00000568503.1:n.607C>T
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000454598
  ensembl transcript: ENST00000568146
  gene symbol: NOL3
  hgvsc: ENST00000568146.1:c.340C>T
  hgvsp: ENSP00000454598.1:p.His114Tyr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000268605
  ensembl transcript: ENST00000268605
  gene symbol: NOL3
  hgvsc: ENST00000268605.7:c.350C>T
  hgvsp: ENSP00000268605.7:p.Ala117Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457243
  ensembl transcript: ENST00000564053
  gene symbol: NOL3
  hgvsc: ENST00000564053.1:c.536C>T
  hgvsp: ENSP00000457243.1:p.Ala179Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457720
  ensembl transcript: ENST00000564992
  gene symbol: NOL3
  hgvsc: ENST00000564992.1:c.350C>T
  hgvsp: ENSP00000457720.1:p.Ala117Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000399831
  ensembl transcript: ENST00000432069
  gene symbol: NOL3
  hgvsc: ENST00000432069.2:c.350C>T
  hgvsp: ENSP00000399831.2:p.Ala117Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000455808
  ensembl transcript: ENST00000566871
  gene symbol: NOL3
  hgvsc: ENST00000566871.1:c.330C>T
  hgvsp: ENSP00000455808.1:p.His111Tyr
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000463698
  ensembl transcript: ENST00000563258
  gene symbol: NOL3
  hgvsc: ENST00000563258.1:c.118C>T
  hgvsp: ENSP00000463698.1:p.Ala40Val
  variant of: http://identifiers.org/hgnc/7869
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000140939
  ensembl protein: ENSP00000457732
  ensembl transcript: ENST00000565560
  gene symbol: NOL3
  hgvsc: ENST00000565560.1:c.350C>T
  hgvsp: ENSP00000457732.1:p.Ala117Val
  variant of: http://identifiers.org/hgnc/7869
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2032
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8207
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1355
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4945
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 12095
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1854
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
hgvs: p.His114Tyr
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 10891
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 107
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 220
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 513
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 918
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1576
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1845
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 34767
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1404
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 312
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10064
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 728
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5004
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7214
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.779232794818874e-5
allele num: 56204
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7626
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.18118e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

VQSLOD
type: SiteQuality
SIO_000300: -4.001e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.153e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.854e0

FS
type: SiteQuality
SIO_000300: 6.52e0

GenotypeQuality
all individuals: 583
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1985
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 173
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 234
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1741
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1508
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2017
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 30557
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 511
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 982
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 14611
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1128
bin: 5.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7178
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.456452082726478e-4
allele num: 6866
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9430
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14620
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4618
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 704
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 5.618398381901266e-5
allele num: 53396
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.07e-1

DP
type: SiteQuality
SIO_000300: 1.114379e6

QD
type: SiteQuality
SIO_000300: 1.209e1

FS
type: SiteQuality
SIO_000300: 2.41e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

MQRankSum
type: SiteQuality
SIO_000300: -2.82e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.07e0

VQSLOD
type: SiteQuality
SIO_000300: 7.14e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

GenotypeQuality
all individuals: 2058
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14969
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2034
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1198
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 29929
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1788
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1067
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 350
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1546
bin: 3.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9356
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6806
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.886436521411054e-5
allele num: 53010
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4568
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7122
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.871907641561298e-5
allele num: 14552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

MQRankSum
type: SiteQuality
SIO_000300: -3.45e-1

QD
type: SiteQuality
SIO_000300: 1.101e1

FS
type: SiteQuality
SIO_000300: 5.985e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.01e-1

DP
type: SiteQuality
SIO_000300: 1.107208e6

GenotypeQuality
all individuals: 1546
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2761
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 350
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1198
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2034
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1067
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2058
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 29929
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1788
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 1.25e1
variant carriers: 1

GenotypeQuality
all individuals: 16
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 497
bin: 7.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53010
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.37438152831226e-4
allele num: 14552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 698
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7122
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6806
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9356
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4568
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.26e0

DP
type: SiteQuality
SIO_000300: 1.107208e6

FS
type: SiteQuality
SIO_000300: 5.985e0

ClippingRankSum
type: SiteQuality
SIO_000300: 5.01e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

VQSLOD
type: SiteQuality
SIO_000300: 4.99e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.45e-1

QD
type: SiteQuality
SIO_000300: 1.101e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.56e-1

GenotypeQuality
all individuals: 984
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 5.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 2417
bin: 6.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9128
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 51964
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4450
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.498800959232614e-4
allele num: 6672
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14426
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.606e0

VQSLOD
type: SiteQuality
SIO_000300: -7.077e-1

DP
type: SiteQuality
SIO_000300: 1.083864e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.4e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.71e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.811e0

QD
type: SiteQuality
SIO_000300: 1.014e1

FS
type: SiteQuality
SIO_000300: 9.587e0

MQRankSum
type: SiteQuality
SIO_000300: 6.73e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.014666774115561e-5
allele num: 49636
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 666
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6382
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4134
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14120
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6624
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -4.66e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.0329e6

BaseQRankSum
type: SiteQuality
SIO_000300: 1.68e0

VQSLOD
type: SiteQuality
SIO_000300: -4.713e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.2e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 2.9e-1

QD
type: SiteQuality
SIO_000300: 7.41e0

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 15
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variant carriers: 6

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14048
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4108
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8524
num of homozygotes: 0

East Asian
type: Population
allele count: 6
allele frequency: 9.157509157509158e-4
allele num: 6552
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 49148
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 658
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.37e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.92e-1

QD
type: SiteQuality
SIO_000300: 1.38e1

DP
type: SiteQuality
SIO_000300: 1.022084e6

MQRankSum
type: SiteQuality
SIO_000300: -1.58e-1

FS
type: SiteQuality
SIO_000300: 6.78e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.53e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1002
bin: 5.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14022
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6230
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 48952
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.539408866995074e-4
allele num: 6496
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.059e0

DP
type: SiteQuality
SIO_000300: 1.018978e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -2.34e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

FS
type: SiteQuality
SIO_000300: 8.869999999999999e0

QD
type: SiteQuality
SIO_000300: 7.11e0

GenotypeQuality
all individuals: 19914
bin: 2.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 939
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2007
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.042817453832326e-5
allele num: 48952
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6496
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14022
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6230
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8504
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 654
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 8.869999999999999e0

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.34e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.6e-2

MQRankSum
type: SiteQuality
SIO_000300: 3.2e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

DP
type: SiteQuality
SIO_000300: 1.018978e6

ClippingRankSum
type: SiteQuality
SIO_000300: -3.2e-1

QD
type: SiteQuality
SIO_000300: 7.11e0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6092
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7836
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3750
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 630
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 7.295010213014298e-5
allele num: 13708
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 46304
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

FS
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 3.63e-1

ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.018e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5916
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 45320
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7624
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5812
num of homozygotes: 0

South Asian
type: Population
allele count: 10
allele frequency: 7.358351729212656e-4
allele num: 13590
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3584
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

MQ
type: SiteQuality
SIO_000300: 5.968e1

VQSLOD
type: SiteQuality
SIO_000300: 1.1e0

QD
type: SiteQuality
SIO_000300: 1.118e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.6e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.644e0

FS
type: SiteQuality
SIO_000300: 2.509e0

MQRankSum
type: SiteQuality
SIO_000300: -4.8e-2

DP
type: SiteQuality
SIO_000300: 9.37724e5

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 19688
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44854
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.713502398903359e-4
allele num: 5836
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13514
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3552
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.330849081714134e-4
allele num: 7514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.31807e5

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.66e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.65e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

GenotypeQuality
all individuals: 712
bin: 1.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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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bin: 6.75e1
variant carriers: 1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 904
bin: 4.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5746
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 6.688366700851652e-5
allele num: 44854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3552
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7514
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5836
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e0

VQSLOD
type: SiteQuality
SIO_000300: 5.66e0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 2.5e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

QD
type: SiteQuality
SIO_000300: 6.65e0

DP
type: SiteQuality
SIO_000300: 9.31807e5

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.23e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 11
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7416
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5768
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5698
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13456
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.253368786335572e-5
allele num: 44378
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.94e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.94e-1

DP
type: SiteQuality
SIO_000300: 9.24283e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.371e0

QD
type: SiteQuality
SIO_000300: 1.925e1

MQ
type: SiteQuality
SIO_000300: 5.875e1

FS
type: SiteQuality
SIO_000300: 2.869e0

VQSLOD
type: SiteQuality
SIO_000300: -2.638e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.5e-3

GenotypeQuality
all individuals: 978
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.736714136853074e-4
allele num: 5758
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5694
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13414
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 602
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 44170
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7364
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3494
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.21e0

MQRankSum
type: SiteQuality
SIO_000300: 4.12e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.67e-1

DP
type: SiteQuality
SIO_000300: 9.16256e5

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.330000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.336e1

FS
type: SiteQuality
SIO_000300: 1.9e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.3e-1

GenotypeQuality
all individuals: 1053
bin: 5.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 2691
bin: 7.5e0
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5568
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 43252
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 584
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13310
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3368
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.396648044692737e-4
allele num: 7160
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.46e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.658e0

MQRankSum
type: SiteQuality
SIO_000300: 8.54e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.065e0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.51e1

MQ
type: SiteQuality
SIO_000300: 5.89e1

DP
type: SiteQuality
SIO_000300: 9.01494e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.900000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: -3.2e-1

GenotypeQuality
all individuals: 149
bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5446
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6854
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3244
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 570
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.844337882700111e-4
allele num: 5422
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 42122
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 13104
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.967e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.200000000000001e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 5.47e-1

DP
type: SiteQuality
SIO_000300: 8.76773e5

QD
type: SiteQuality
SIO_000300: 1.135e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.05e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.46e-1

FS
type: SiteQuality
SIO_000300: 1.308e0

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

GenotypeQuality
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bin: 3.25e1
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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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: 8.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4920
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6148
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5042
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2934
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 12722
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 540
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.571751877378871e-5
allele num: 38884
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.7e-3

VQSLOD
type: SiteQuality
SIO_000300: 8.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.932e0

MQRankSum
type: SiteQuality
SIO_000300: 1.41e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

QD
type: SiteQuality
SIO_000300: 1.243e1

DP
type: SiteQuality
SIO_000300: 8.13273e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.64e0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4604
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4742
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 8.084074373484237e-5
allele num: 12370
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5716
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 508
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European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2696
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 36404
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.56e0

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -1.13e-2

BaseQRankSum
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SIO_000300: -1.868e0

MQRankSum
type: SiteQuality
SIO_000300: 1.4e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.78e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 7.7108e5

VQSLOD
type: SiteQuality
SIO_000300: -2.818e-1

GenotypeQuality
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bin: 2.5e0
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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GenotypeQuality
all individuals: 28
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 100
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GenotypeQuality
all individuals: 698
bin: 1.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5440
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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Other
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African
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allele frequency: 0.0e0
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East Asian
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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ReadPosRankSum
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QD
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MQRankSum
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MQ
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FS
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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DP
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele frequency: 0.0e0
allele num: 4918
num of homozygotes: 0

Other
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allele frequency: 0.0e0
allele num: 462
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 8.504847763225038e-5
allele num: 11758
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 3.104625892579944e-5
allele num: 32210
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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QD
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MQ
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ReadPosRankSum
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FS
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DP
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MQRankSum
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 2.710027100271003e-4
allele num: 3690
num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
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Latino
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 3
allele frequency: 9.999333377774815e-5
allele num: 30002
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European (Finnish)
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allele frequency: 0.0e0
allele num: 2000
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MQ
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SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: 5.73e-1

VQSLOD
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ReadPosRankSum
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FS
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DP
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InbreedingCoeff
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MQRankSum
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ClippingRankSum
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QD
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 3366
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.571938848406915e-5
allele num: 27996
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 4044
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 3522
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 420
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VQSLOD
type: SiteQuality
SIO_000300: -1.5e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.89e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.7e-2

DP
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SIO_000300: 6.45048e5

MQRankSum
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MQ
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 2.688e0

BaseQRankSum
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SIO_000300: 2.08e0

QD
type: SiteQuality
SIO_000300: 3.69e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.31e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 10320
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 8.791981712678038e-5
allele num: 22748
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 2580
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European (Finnish)
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allele count: 0
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allele num: 1244
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MQRankSum
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SIO_000300: -1.002e0

ClippingRankSum
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DP
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InbreedingCoeff
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SIO_000300: -2.4e-2

QD
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FS
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ReadPosRankSum
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MQ
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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allele frequency: 5.907837731390311e-4
allele num: 10156
num of homozygotes: 0

Latino
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allele frequency: 1.457725947521866e-3
allele num: 2744
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African
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allele frequency: 7.627765064836003e-4
allele num: 2622
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European (Finnish)
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allele num: 1106
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Other
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European (Non-Finnish)
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allele frequency: 2.620741295394983e-3
allele num: 21368
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East Asian
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ClippingRankSum
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VQSLOD
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MQ
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MQRankSum
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FS
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InbreedingCoeff
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BaseQRankSum
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DP
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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Other
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East Asian
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African
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Latino
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European (Non-Finnish)
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South Asian
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InbreedingCoeff
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ClippingRankSum
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FS
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BaseQRankSum
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VQSLOD
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QD
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ReadPosRankSum
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MQ
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DP
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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East Asian
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Latino
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African
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European (Non-Finnish)
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MQRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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ClippingRankSum
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MQ
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DP
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InbreedingCoeff
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VQSLOD
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

Other
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allele count: 0
allele frequency: 0.0e0
allele num: 260
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1700
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 6.724949562878279e-5
allele num: 14870
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1458
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 582
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.055e1

MQRankSum
type: SiteQuality
SIO_000300: 6.889999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.03e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.31e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.55e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

DP
type: SiteQuality
SIO_000300: 4.83373e5

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.25e1
variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 1682
num of homozygotes: 0

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 254
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14566
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 1656
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 580
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.31e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
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SIO_000300: -7.31e-1

DP
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SIO_000300: 4.80044e5

QD
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SIO_000300: 1.312e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.67e-2

ReadPosRankSum
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SIO_000300: 7.31e-1

VQSLOD
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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 (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 13448
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 1272
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 228
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1594
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: 4.6555e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.68e0

QD
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.73e-1

VQSLOD
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SIO_000300: -1.226e0

InbreedingCoeff
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SIO_000300: -3.75e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.73e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 3.01e0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 8.254911672445105e-5
allele num: 12114
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 450
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 212
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1174
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7764
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1446
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.48e-1

FS
type: SiteQuality
SIO_000300: 1.445e0

MQRankSum
type: SiteQuality
SIO_000300: 5.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.82e-1

QD
type: SiteQuality
SIO_000300: 6.12e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

VQSLOD
type: SiteQuality
SIO_000300: -3.219e-1

DP
type: SiteQuality
SIO_000300: 4.44691e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.88e-2

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 934
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1184
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 964
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 5.923000987166831e-4
allele num: 10130
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 3.2e-4
allele num: 6250
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 366
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 180
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.07e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
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SIO_000300: -1.893e0

FS
type: SiteQuality
SIO_000300: 5.55e0

MQRankSum
type: SiteQuality
SIO_000300: -3.12e-1

QD
type: SiteQuality
SIO_000300: 1.066e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.77e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.903e-1

DP
type: SiteQuality
SIO_000300: 4.00402e5

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

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

South Asian
type: Population
allele count: 2
allele frequency: 3.68052999631947e-4
allele num: 5434
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 1114
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9424
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
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BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

QD
type: SiteQuality
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MQRankSum
type: SiteQuality
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FS
type: SiteQuality
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DP
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: 6.95e-1

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9424
num of homozygotes: 0

African
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allele frequency: 8.976660682226212e-4
allele num: 1114
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

East Asian
type: Population
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5434
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 322
num of homozygotes: 0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 5.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 324
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 9386
num of homozygotes: 0

South Asian
type: Population
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East Asian
type: Population
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allele frequency: 0.0e0
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African
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Other
type: Population
allele count: 0
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allele num: 160
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 894
num of homozygotes: 0

FS
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MQRankSum
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QD
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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ReadPosRankSum
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MQ
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InbreedingCoeff
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SIO_000300: 3.47e-2

DP
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Latino
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East Asian
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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FS
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MQRankSum
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QD
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MQ
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Other
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Latino
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European (Finnish)
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African
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South Asian
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East Asian
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ClippingRankSum
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FS
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MQ
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QD
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InbreedingCoeff
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BaseQRankSum
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VQSLOD
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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African
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European (Finnish)
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South Asian
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East Asian
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Latino
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European (Non-Finnish)
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FS
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QD
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VQSLOD
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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BaseQRankSum
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MQ
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MQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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European (Non-Finnish)
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Other
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VQSLOD
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FS
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ReadPosRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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DP
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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Latino
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European (Finnish)
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European (Non-Finnish)
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East Asian
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Other
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FS
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MQ
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InbreedingCoeff
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QD
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BaseQRankSum
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DP
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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Other
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South Asian
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Latino
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European (Finnish)
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African
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European (Non-Finnish)
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QD
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ClippingRankSum
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BaseQRankSum
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MQRankSum
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DP
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MQ
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FS
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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European (Finnish)
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South Asian
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European (Non-Finnish)
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East Asian
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Latino
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Other
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ReadPosRankSum
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BaseQRankSum
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QD
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MQRankSum
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MQ
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FS
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ClippingRankSum
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InbreedingCoeff
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VQSLOD
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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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South Asian
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East Asian
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African
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European (Finnish)
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European (Non-Finnish)
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Latino
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Other
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FS
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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VQSLOD
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 924
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7694
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 352
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1150
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 74
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 998
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 816
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.728e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.16e-2

DP
type: SiteQuality
SIO_000300: 3.39175e5

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -6.188e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.495e0

QD
type: SiteQuality
SIO_000300: 1.028e1

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 1

GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 16

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
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GenotypeQuality
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bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1124
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 110
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1314
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1054
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 496
num of homozygotes: 0

East Asian
type: Population
allele count: 14
allele frequency: 1.140065146579805e-2
allele num: 1228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.153316106804479e-4
allele num: 9288
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.8e-1

FS
type: SiteQuality
SIO_000300: 4.584e0

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
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DP
type: SiteQuality
SIO_000300: 3.67505e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.76e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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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bin: 5.25e1
variant carriers: 1

European (Non-Finnish)
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allele count: 2
allele frequency: 3.839361130307917e-5
allele num: 52092
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.336898395721925e-4
allele num: 7480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7022
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.008064516129032e-4
allele num: 9920
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4596
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6824
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

QD
type: SiteQuality
SIO_000300: 9.76e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.33e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

FS
type: SiteQuality
SIO_000300: 2.258e0

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

DP
type: SiteQuality
SIO_000300: 8.93933e5

GenotypeQuality
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variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4596
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6824
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.008064516129032e-4
allele num: 9920
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7480
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7022
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 52092
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

QD
type: SiteQuality
SIO_000300: 9.76e0

DP
type: SiteQuality
SIO_000300: 8.93933e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.258e0

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.33e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3.839361130307917e-5
allele num: 52092
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 5
allele frequency: 1.087902523933855e-3
allele num: 4596
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7022
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7480
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6824
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

FS
type: SiteQuality
SIO_000300: 2.258e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.17e-1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 3.33e-2

DP
type: SiteQuality
SIO_000300: 8.93933e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.98e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.44e-1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 7624
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 604
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4654
num of homozygotes: 0

Latino
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allele count: 3
allele frequency: 2.969121140142518e-4
allele num: 10104
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 52996
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 6960
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ClippingRankSum
type: SiteQuality
SIO_000300: -1.54e-1

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 4672
num of homozygotes: 0

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

South Asian
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num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 610
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.885440627474641e-5
allele num: 53038
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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MQ
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FS
type: SiteQuality
SIO_000300: 2.218e0

MQRankSum
type: SiteQuality
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VQSLOD
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DP
type: SiteQuality
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QD
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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 4672
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
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allele num: 53058
num of homozygotes: 0

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

South Asian
type: Population
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allele frequency: 0.0e0
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African
type: Population
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Other
type: Population
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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QD
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MQ
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VQSLOD
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ClippingRankSum
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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
all individuals: 2791
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 361
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2718
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 19
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26503
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 651
bin: 5.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 53620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10248
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7714
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7040
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4762
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.371742112482853e-4
allele num: 7290
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -9.02e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 5.969e0

MQRankSum
type: SiteQuality
SIO_000300: -3.18e-1

QD
type: SiteQuality
SIO_000300: 2.325e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.899999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.047e0

DP
type: SiteQuality
SIO_000300: 9.90673e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.65e-1

GenotypeQuality
all individuals: 7139
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 130
bin: 9.75e1
variant carriers: 80

GenotypeQuality
all individuals: 2747
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 623
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 551
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1758
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 7.75e1
variant carriers: 4

GenotypeQuality
all individuals: 578
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32290
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3076
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 593
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 393
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1967
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 131
bin: 8.25e1
variant carriers: 7

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.43090760425184e-3
allele num: 4892
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.791736460078169e-4
allele num: 7164
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 72
allele frequency: 1.312623058411726e-3
allele num: 54852
num of homozygotes: 0

Latino
type: Population
allele count: 8
allele frequency: 7.646721468170522e-4
allele num: 10462
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7856
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 5.353319057815846e-4
allele num: 7472
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 3.215434083601286e-3
allele num: 622
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -1.952e0

FS
type: SiteQuality
SIO_000300: 6.95e-1

MQ
type: SiteQuality
SIO_000300: 5.567e1

QD
type: SiteQuality
SIO_000300: 7.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.42e-1

DP
type: SiteQuality
SIO_000300: 1.05606e6

GenotypeQuality
all individuals: 488
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 9.75e1
variant carriers: 82

GenotypeQuality
all individuals: 396
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 602
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 605
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 8.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1814
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4996
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 33153
bin: 6.25e1
variant carriers: 1

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7034
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 539
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2428
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 8
allele frequency: 7.630675314765357e-4
allele num: 10484
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.78473962684489e-4
allele num: 7182
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 72
allele frequency: 1.312527344319673e-3
allele num: 54856
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 5.331911490269261e-4
allele num: 7502
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 7
allele frequency: 1.427988576091391e-3
allele num: 4902
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7898
num of homozygotes: 0

Other
type: Population
allele count: 2
allele frequency: 3.205128205128205e-3
allele num: 624
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.067884e6

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.427e0

MQ
type: SiteQuality
SIO_000300: 5.589e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.45e-2

FS
type: SiteQuality
SIO_000300: 6.73e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.88e0

QD
type: SiteQuality
SIO_000300: 5.6e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.88e-1

GenotypeQuality
all individuals: 486
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 539
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 445
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 135
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7034
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 488
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 602
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 605
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variant carriers: 0

GenotypeQuality
all individuals: 1814
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 396
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variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3157
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1533
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 5.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7182
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4902
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.822954644888435e-5
allele num: 54856
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7898
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 624
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7502
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.589e1

FS
type: SiteQuality
SIO_000300: 6.73e-1

DP
type: SiteQuality
SIO_000300: 1.067884e6

QD
type: SiteQuality
SIO_000300: 5.6e0

VQSLOD
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: -1.88e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.45e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 2.88e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.427e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.0e0

GenotypeQuality
all individuals: 4978
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 556
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7011
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 507
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 512
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1767
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variant carriers: 0

GenotypeQuality
all individuals: 2338
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3227
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33388
bin: 6.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7514
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 54940
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10500
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.262626262626263e-4
allele num: 7920
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7204
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4918
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.552e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-3

QD
type: SiteQuality
SIO_000300: 3.126e1

MQ
type: SiteQuality
SIO_000300: 5.58e1

VQSLOD
type: SiteQuality
SIO_000300: -6.968e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -8.169999999999999e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.47e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.47e-1

DP
type: SiteQuality
SIO_000300: 1.072667e6

GenotypeQuality
all individuals: 432
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 475
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 492
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 53
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variant carriers: 0

GenotypeQuality
all individuals: 479
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 494
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variant carriers: 0

GenotypeQuality
all individuals: 6859
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4869
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1249
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
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variant carriers: 0

GenotypeQuality
all individuals: 3311
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 659
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 616
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34509
bin: 6.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10564
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 628
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7266
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.316482359136387e-4
allele num: 7596
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4956
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7972
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 55372
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -1.14e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.8e-3

FS
type: SiteQuality
SIO_000300: 3.741e0

VQSLOD
type: SiteQuality
SIO_000300: -1.634e0

DP
type: SiteQuality
SIO_000300: 1.090023e6

QD
type: SiteQuality
SIO_000300: 5.38e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.580000000000001e-1

GenotypeDepth
all individuals: 1310
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 552
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 472
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6538
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 312
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3703
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 905
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 465
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4236
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 930
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 467
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 309
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 598
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 765
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38430
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 29
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8130
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.250625312656328e-4
allele num: 7996
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.758767455766999e-5
allele num: 56858
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 650
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10806
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5178
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.21e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.28e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.7e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -6.840000000000001e-1

QD
type: SiteQuality
SIO_000300: 9.380000000000001e0

FS
type: SiteQuality
SIO_000300: 2.395e0

DP
type: SiteQuality
SIO_000300: 1.151763e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.8e-3

VQSLOD
type: SiteQuality
SIO_000300: 7.18e-1

GenotypeQuality
all individuals: 54
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 292
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6969
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 802
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39508
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3849
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3608
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 374
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 570
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 498
bin: 5.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10892
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8300
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7670
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5278
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 660
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.482257896019779e-5
allele num: 57434
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.69e-1

QD
type: SiteQuality
SIO_000300: 1.063e1

FS
type: SiteQuality
SIO_000300: 4.16e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.3e-3

DP
type: SiteQuality
SIO_000300: 1.177222e6

MQRankSum
type: SiteQuality
SIO_000300: 9.14e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

VQSLOD
type: SiteQuality
SIO_000300: 6.09e-1

GenotypeQuality
all individuals: 8050
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 266
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 421
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 727
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 310
bin: 4.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 548
bin: 7.75e1
variant carriers: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10942
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 676
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.213592233009709e-4
allele num: 8240
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5314
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57840
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7774
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8914
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.197573e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.77e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.52e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.831e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.587e0

FS
type: SiteQuality
SIO_000300: 4.981e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.2e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.102e0

MQRankSum
type: SiteQuality
SIO_000300: -8.32e-1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

Latino
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allele count: 6
allele frequency: 5.486466715435259e-4
allele num: 10936
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8242
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9180
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 25
allele frequency: 4.319729066592943e-4
allele num: 57874
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5280
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7770
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 2.71e0

FS
type: SiteQuality
SIO_000300: 2.454e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

DP
type: SiteQuality
SIO_000300: 1.197973e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.12e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.3e-2

QD
type: SiteQuality
SIO_000300: 1.202e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

African
type: Population
allele count: 2
allele frequency: 2.577319587628866e-4
allele num: 7760
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9194
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57640
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5242
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.751e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.71e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.8e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.29e0

VQSLOD
type: SiteQuality
SIO_000300: -7.479e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.28e0

MQRankSum
type: SiteQuality
SIO_000300: 7.75e-1

DP
type: SiteQuality
SIO_000300: 1.192885e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 7.82e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 3876
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GenotypeQuality
all individuals: 32
bin: 8.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10916
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9302
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 682
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57712
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8226
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.288327750579748e-4
allele num: 7762
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5242
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 1.059e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.557e0

DP
type: SiteQuality
SIO_000300: 1.194047e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.02e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -1.507e0

VQSLOD
type: SiteQuality
SIO_000300: -1.003e0

MQ
type: SiteQuality
SIO_000300: 5.875e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 21
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GenotypeQuality
all individuals: 150
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variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10862
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57536
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5194
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7692
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.219809709685289e-4
allele num: 8198
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9504
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.18865e6

VQSLOD
type: SiteQuality
SIO_000300: 8.27e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.2e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -5.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.77e-1

FS
type: SiteQuality
SIO_000300: 7.78e-1

QD
type: SiteQuality
SIO_000300: 1.353e1

MQRankSum
type: SiteQuality
SIO_000300: 7.17e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.25e0

GenotypeQuality
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variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10858
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.220703125e-4
allele num: 8192
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 57498
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5198
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -4.13e-1

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.903e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 4.195e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.739190928380118e-5
allele num: 57498
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8192
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7698
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5198
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10858
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.964e-1

MQRankSum
type: SiteQuality
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MQ
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.189013e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

QD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 4.195e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e-1

ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 29
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GenotypeQuality
all individuals: 141
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GenotypeQuality
all individuals: 486
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GenotypeQuality
all individuals: 18
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variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 690
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8194
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 57
allele frequency: 9.910285833507199e-4
allele num: 57516
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10862
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.849114703618168e-4
allele num: 5196
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.030290541932825e-4
allele num: 9706
num of homozygotes: 0

African
type: Population
allele count: 4
allele frequency: 5.192107995846313e-4
allele num: 7704
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.71e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.3e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.156e1

FS
type: SiteQuality
SIO_000300: 5.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.28e-1

DP
type: SiteQuality
SIO_000300: 1.18887e6

ClippingRankSum
type: SiteQuality
SIO_000300: 3.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.32e-1

GenotypeQuality
all individuals: 18
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1336
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 240
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 9654
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 751
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 373
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 630
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1804
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3604
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1088
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 267
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 784
bin: 5.75e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10770
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7626
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.746969008769784e-5
allele num: 57242
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5158
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9778
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 684
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 5.36e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.4e-1

QD
type: SiteQuality
SIO_000300: 6.72e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

DP
type: SiteQuality
SIO_000300: 1.180059e6

FS
type: SiteQuality
SIO_000300: 1.191e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.68e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.8e-1