9-95077971-AATC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95077971
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95077968
    reference: chr 9
allele count: 7
allele frequency: 6.268357332187119e-5
allele num: 111672
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1225_*1227delGAT
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.933_935delGAT
  hgvsp: ENSP00000412471.2:p.Met311del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*788_*790delGAT
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*788_*790delGAT
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.729_731delGAT
  hgvsp: ENSP00000351723.4:p.Met243del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.933_935delGAT
  hgvsp: ENSP00000441300.1:p.Met311del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.933_935delGAT
  hgvsp: ENSP00000414112.2:p.Met311del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.729_731delGAT
  hgvsp: ENSP00000440709.1:p.Met243del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.777_779delGAT
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.933_935delGAT
  hgvsp: ENSP00000441140.1:p.Met311del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.933_935delGAT
  hgvsp: ENSP00000439751.1:p.Met311del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.933_935delGAT
  hgvsp: ENSP00000401177.2:p.Met311del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4433_282-4431delGAT
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9910
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 22739
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8675
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 506
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Met311del
num of homozygotes: 0
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: Other
reference allele: AATC
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum

9-95077972-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95077972
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95077972
    reference: chr 9
allele count: 2
allele frequency: 1.790542355279414e-5
allele num: 111698
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4431T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.935T>C
  hgvsp: ENSP00000439751.1:p.Ile312Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.731T>C
  hgvsp: ENSP00000440709.1:p.Ile244Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*790T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.935T>C
  hgvsp: ENSP00000414112.2:p.Ile312Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.935T>C
  hgvsp: ENSP00000401177.2:p.Ile312Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1227T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.731T>C
  hgvsp: ENSP00000351723.4:p.Ile244Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.779T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.935T>C
  hgvsp: ENSP00000412471.2:p.Ile312Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*790T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.935T>C
  hgvsp: ENSP00000441300.1:p.Ile312Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.935T>C
  hgvsp: ENSP00000441140.1:p.Ile312Thr
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4188
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22863
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 223
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9695
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1810
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile312Thr
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: MQ

9-95077982-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95077982
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95077982
    reference: chr 9
allele count: 1
allele frequency: 8.945503989694779e-6
allele num: 111788
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.721A>T
  hgvsp: ENSP00000351723.4:p.Arg241Ter
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.925A>T
  hgvsp: ENSP00000441140.1:p.Arg309Ter
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*780A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.721A>T
  hgvsp: ENSP00000440709.1:p.Arg241Ter
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.925A>T
  hgvsp: ENSP00000441300.1:p.Arg309Ter
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.925A>T
  hgvsp: ENSP00000412471.2:p.Arg309Ter
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.925A>T
  hgvsp: ENSP00000401177.2:p.Arg309Ter
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.925A>T
  hgvsp: ENSP00000414112.2:p.Arg309Ter
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.925A>T
  hgvsp: ENSP00000439751.1:p.Arg309Ter
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4441A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.769A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1217A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*780A>T
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10000
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7633
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24135
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 509
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9317
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg309Ter
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

9-95077998-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95077998
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95077998
    reference: chr 9
allele count: 5
allele frequency: 4.447448943286131e-5
allele num: 112424
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.909T>C
  hgvsp: ENST00000545558.1:c.909T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.909T>C
  hgvsp: ENST00000544867.1:c.909T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.909T>C
  hgvsp: ENST00000442668.2:c.909T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*764T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4457T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1201T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.909T>C
  hgvsp: ENST00000535387.1:c.909T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.705T>C
  hgvsp: ENST00000542053.1:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.705T>C
  hgvsp: ENST00000358855.4:c.705T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.909T>C
  hgvsp: ENST00000432670.2:c.909T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*764T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.909T>C
  hgvsp: ENST00000433029.2:c.909T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.753T>C
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10591
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8275
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Asp303Asp
num of homozygotes: 0
population: African
population: Latino
population: Other
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-95078003-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078003
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078003
    reference: chr 9
allele count: 1
allele frequency: 8.875161971705983e-6
allele num: 112674
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.904A>G
  hgvsp: ENSP00000412471.2:p.Thr302Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*759A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.904A>G
  hgvsp: ENSP00000441140.1:p.Thr302Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*759A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.904A>G
  hgvsp: ENSP00000441300.1:p.Thr302Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.904A>G
  hgvsp: ENSP00000414112.2:p.Thr302Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.700A>G
  hgvsp: ENSP00000351723.4:p.Thr234Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.700A>G
  hgvsp: ENSP00000440709.1:p.Thr234Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.904A>G
  hgvsp: ENSP00000401177.2:p.Thr302Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.748A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1196A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.904A>G
  hgvsp: ENSP00000439751.1:p.Thr302Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4462A>G
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27225
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1902
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 1.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Thr302Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum

9-95078003-TATC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078003
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078000
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 112674
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.901_903delGAT
  hgvsp: ENSP00000412471.2:p.Asp301del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*756_*758delGAT
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.697_699delGAT
  hgvsp: ENSP00000351723.4:p.Asp233del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.745_747delGAT
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.901_903delGAT
  hgvsp: ENSP00000439751.1:p.Asp301del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4465_282-4463delGAT
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.901_903delGAT
  hgvsp: ENSP00000401177.2:p.Asp301del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1193_*1195delGAT
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.901_903delGAT
  hgvsp: ENSP00000441300.1:p.Asp301del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.697_699delGAT
  hgvsp: ENSP00000440709.1:p.Asp233del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.901_903delGAT
  hgvsp: ENSP00000441140.1:p.Asp301del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*756_*758delGAT
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.901_903delGAT
  hgvsp: ENSP00000414112.2:p.Asp301del
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: inframe deletion
filter: AC_Adj0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5525
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10816
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3796
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7844
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp301del
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: African
reference allele: TATC
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum

9-95078005-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078005
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078005
    reference: chr 9
allele count: 1
allele frequency: 8.866348660294717e-6
allele num: 112786
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.902A>T
  hgvsp: ENSP00000414112.2:p.Asp301Val
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.698A>T
  hgvsp: ENSP00000440709.1:p.Asp233Val
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4464A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.698A>T
  hgvsp: ENSP00000351723.4:p.Asp233Val
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.902A>T
  hgvsp: ENSP00000412471.2:p.Asp301Val
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.902A>T
  hgvsp: ENSP00000441300.1:p.Asp301Val
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.902A>T
  hgvsp: ENSP00000439751.1:p.Asp301Val
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*757A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.902A>T
  hgvsp: ENSP00000441140.1:p.Asp301Val
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.746A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*757A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1194A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.902A>T
  hgvsp: ENSP00000401177.2:p.Asp301Val
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7670
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3747
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10903
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp301Val
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: QD

9-95078007-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078007
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078007
    reference: chr 9
allele count: 1
allele frequency: 8.854886126164418e-6
allele num: 112932
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.900T>C
  hgvsp: ENST00000432670.2:c.900T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4466T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.900T>C
  hgvsp: ENST00000433029.2:c.900T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*755T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.900T>C
  hgvsp: ENST00000545558.1:c.900T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*755T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.696T>C
  hgvsp: ENST00000358855.4:c.696T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.696T>C
  hgvsp: ENST00000542053.1:c.696T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1192T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.900T>C
  hgvsp: ENST00000544867.1:c.900T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.744T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.900T>C
  hgvsp: ENST00000442668.2:c.900T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.900T>C
  hgvsp: ENST00000535387.1:c.900T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10999
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7539
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27646
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3697
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1925
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp300Asp
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: MQ
site quality: QD

9-95078011-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078011
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078011
    reference: chr 9
allele count: 1
allele frequency: 8.84016973125884e-6
allele num: 113120
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.896A>C
  hgvsp: ENSP00000412471.2:p.Asp299Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.896A>C
  hgvsp: ENSP00000439751.1:p.Asp299Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.896A>C
  hgvsp: ENSP00000441300.1:p.Asp299Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1188A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.692A>C
  hgvsp: ENSP00000351723.4:p.Asp231Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.896A>C
  hgvsp: ENSP00000401177.2:p.Asp299Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.896A>C
  hgvsp: ENSP00000441140.1:p.Asp299Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.896A>C
  hgvsp: ENSP00000414112.2:p.Asp299Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*751A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.692A>C
  hgvsp: ENSP00000440709.1:p.Asp231Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4470A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*751A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.740A>C
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11118
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28371
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4906
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7183
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3608
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1935
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp299Ala
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum

9-95078022-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078022
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078022
    reference: chr 9
allele count: 1
allele frequency: 8.79445597495339e-6
allele num: 113708
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.885C>G
  hgvsp: ENSP00000412471.2:p.Asn295Lys
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.681C>G
  hgvsp: ENSP00000440709.1:p.Asn227Lys
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*740C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.885C>G
  hgvsp: ENSP00000414112.2:p.Asn295Lys
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1177C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.885C>G
  hgvsp: ENSP00000441300.1:p.Asn295Lys
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.885C>G
  hgvsp: ENSP00000439751.1:p.Asn295Lys
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4481C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.681C>G
  hgvsp: ENSP00000351723.4:p.Asn227Lys
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.729C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*740C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.885C>G
  hgvsp: ENSP00000441140.1:p.Asn295Lys
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.885C>G
  hgvsp: ENSP00000401177.2:p.Asn295Lys
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 121
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11617
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4357
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6174
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3310
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asn295Lys
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

9-95078025-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078025
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078025
    reference: chr 9
allele count: 5
allele frequency: 4.38889083950704e-5
allele num: 113924
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.882A>G
  hgvsp: ENST00000535387.1:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.882A>G
  hgvsp: ENST00000432670.2:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*737A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*737A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.882A>G
  hgvsp: ENST00000545558.1:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1174A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4484A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.882A>G
  hgvsp: ENST00000442668.2:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.678A>G
  hgvsp: ENST00000542053.1:c.678A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.678A>G
  hgvsp: ENST00000358855.4:c.678A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.882A>G
  hgvsp: ENST00000544867.1:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.882A>G
  hgvsp: ENST00000433029.2:c.882A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.726A>G
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4296
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29924
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5928
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11748
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg294Arg
num of homozygotes: 0
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: MQ

9-95078032-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078032
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078032
    reference: chr 9
allele count: 3
allele frequency: 2.622927886969294e-5
allele num: 114376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4491A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1167A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.875A>C
  hgvsp: ENSP00000414112.2:p.Lys292Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.875A>C
  hgvsp: ENSP00000412471.2:p.Lys292Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*730A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.875A>C
  hgvsp: ENSP00000441300.1:p.Lys292Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.719A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.875A>C
  hgvsp: ENSP00000401177.2:p.Lys292Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.671A>C
  hgvsp: ENSP00000440709.1:p.Lys224Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.671A>C
  hgvsp: ENSP00000351723.4:p.Lys224Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.875A>C
  hgvsp: ENSP00000439751.1:p.Lys292Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*730A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.875A>C
  hgvsp: ENSP00000441140.1:p.Lys292Thr
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 12184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3934
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 30675
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3018
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5297
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys292Thr
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: VQSLOD

9-95078033-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078033
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078033
    reference: chr 9
allele count: 1
allele frequency: 8.736676568233443e-6
allele num: 114460
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*729A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.874A>G
  hgvsp: ENSP00000439751.1:p.Lys292Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.670A>G
  hgvsp: ENSP00000351723.4:p.Lys224Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.874A>G
  hgvsp: ENSP00000401177.2:p.Lys292Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.874A>G
  hgvsp: ENSP00000441140.1:p.Lys292Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1166A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.670A>G
  hgvsp: ENSP00000440709.1:p.Lys224Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*729A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.874A>G
  hgvsp: ENSP00000441300.1:p.Lys292Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.874A>G
  hgvsp: ENSP00000412471.2:p.Lys292Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4492A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.718A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.874A>G
  hgvsp: ENSP00000414112.2:p.Lys292Glu
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5217
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12244
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3841
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2982
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Lys292Glu
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: T
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff

9-95078044-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078044
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078044
    reference: chr 9
allele count: 1
allele frequency: 8.678446210990383e-6
allele num: 115228
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.863T>C
  hgvsp: ENSP00000441300.1:p.Leu288Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1155T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.863T>C
  hgvsp: ENSP00000414112.2:p.Leu288Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.863T>C
  hgvsp: ENSP00000441140.1:p.Leu288Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.863T>C
  hgvsp: ENSP00000439751.1:p.Leu288Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.659T>C
  hgvsp: ENSP00000440709.1:p.Leu220Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4503T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.863T>C
  hgvsp: ENSP00000401177.2:p.Leu288Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.863T>C
  hgvsp: ENSP00000412471.2:p.Leu288Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*718T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.659T>C
  hgvsp: ENSP00000351723.4:p.Leu220Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.707T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*718T>C
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2152
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2613
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13151
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31392
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 516
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4284
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu288Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

9-95078045-AG-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078045
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078044
    reference: chr 9
allele count: 1
allele frequency: 8.674983083782986e-6
allele num: 115274
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.657delC
  hgvsp: ENSP00000440709.1:p.Leu220TrpfsTer21
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.861delC
  hgvsp: ENSP00000441140.1:p.Leu288TrpfsTer21
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.861delC
  hgvsp: ENSP00000414112.2:p.Leu288TrpfsTer21
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.705delC
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*716delC
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.861delC
  hgvsp: ENSP00000439751.1:p.Leu288TrpfsTer21
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.861delC
  hgvsp: ENSP00000412471.2:p.Leu288TrpfsTer21
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.861delC
  hgvsp: ENSP00000441300.1:p.Leu288TrpfsTer21
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1153delC
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*716delC
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.657delC
  hgvsp: ENSP00000351723.4:p.Leu220TrpfsTer21
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.861delC
  hgvsp: ENSP00000401177.2:p.Leu288TrpfsTer21
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4505delC
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2575
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4185
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3508
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2173
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13166
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu288TrpfsTer21
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: Other
reference allele: AG
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: FS
site quality: MQRankSum

9-95078048-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078048
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078048
    reference: chr 9
allele count: 1
allele frequency: 8.652614820198665e-6
allele num: 115572
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.859G>A
  hgvsp: ENSP00000439751.1:p.Gly287Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4507G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.859G>A
  hgvsp: ENSP00000412471.2:p.Gly287Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.655G>A
  hgvsp: ENSP00000351723.4:p.Gly219Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.859G>A
  hgvsp: ENSP00000401177.2:p.Gly287Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1151G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*714G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*714G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.859G>A
  hgvsp: ENSP00000414112.2:p.Gly287Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.859G>A
  hgvsp: ENSP00000441140.1:p.Gly287Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.703G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.655G>A
  hgvsp: ENSP00000440709.1:p.Gly219Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.859G>A
  hgvsp: ENSP00000441300.1:p.Gly287Ser
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3849
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 332
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2429
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2226
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly287Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ

http://identifiers.org/exac.variant/9-95078052-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078052
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078052
    reference: chr 9
allele count: 1
allele frequency: 8.620541025154739e-6
allele num: 116002
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*710T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.699T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.855T>G
  hgvsp: ENST00000442668.2:c.855T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.855T>G
  hgvsp: ENST00000432670.2:c.855T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.855T>G
  hgvsp: ENST00000545558.1:c.855T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1147T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.651T>G
  hgvsp: ENST00000542053.1:c.651T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.855T>G
  hgvsp: ENST00000544867.1:c.855T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.855T>G
  hgvsp: ENST00000535387.1:c.855T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.651T>G
  hgvsp: ENST00000358855.4:c.651T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4511T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*710T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.855T>G
  hgvsp: ENST00000433029.2:c.855T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2201
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2881
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32338
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3483
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 512
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14031
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2254
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Thr285Thr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum

9-95078064-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078064
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078064
    reference: chr 9
allele count: 1
allele frequency: 8.514116404999489e-6
allele num: 117452
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.639A>G
  hgvsp: ENST00000542053.1:c.639A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.843A>G
  hgvsp: ENST00000544867.1:c.843A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.843A>G
  hgvsp: ENST00000432670.2:c.843A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.843A>G
  hgvsp: ENST00000545558.1:c.843A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*698A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.687A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.639A>G
  hgvsp: ENST00000358855.4:c.639A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.843A>G
  hgvsp: ENST00000535387.1:c.843A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4523A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.843A>G
  hgvsp: ENST00000433029.2:c.843A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.843A>G
  hgvsp: ENST00000442668.2:c.843A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1135A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*698A>G
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2014
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2347
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1568
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34714
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu281Leu
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/9-95078065-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078065
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078065
    reference: chr 9
allele count: 2
allele frequency: 1.700709195734621e-5
allele num: 117598
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.638T>G
  hgvsp: ENSP00000440709.1:p.Leu213Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.842T>G
  hgvsp: ENSP00000441300.1:p.Leu281Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.842T>G
  hgvsp: ENSP00000412471.2:p.Leu281Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4524T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.842T>G
  hgvsp: ENSP00000414112.2:p.Leu281Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.638T>G
  hgvsp: ENSP00000351723.4:p.Leu213Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.842T>G
  hgvsp: ENSP00000401177.2:p.Leu281Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.842T>G
  hgvsp: ENSP00000441140.1:p.Leu281Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.842T>G
  hgvsp: ENSP00000439751.1:p.Leu281Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*697T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*697T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1134T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.686T>G
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34907
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1937
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2322
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1310
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu281Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: Other
population: African
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff

9-95078066-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078066
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078066
    reference: chr 9
allele count: 9
allele frequency: 7.646948867401907e-5
allele num: 117694
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.637C>A
  hgvsp: ENSP00000440709.1:p.Leu213Ile
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.841C>A
  hgvsp: ENSP00000412471.2:p.Leu281Ile
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.841C>A
  hgvsp: ENSP00000439751.1:p.Leu281Ile
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.841C>A
  hgvsp: ENSP00000401177.2:p.Leu281Ile
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.685C>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.841C>A
  hgvsp: ENSP00000414112.2:p.Leu281Ile
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.637C>A
  hgvsp: ENSP00000351723.4:p.Leu213Ile
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*696C>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.841C>A
  hgvsp: ENSP00000441140.1:p.Leu281Ile
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1133C>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4525C>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.841C>A
  hgvsp: ENSP00000441300.1:p.Leu281Ile
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*696C>A
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2355
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1851
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1223
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 522
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 241
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu281Ile
num of homozygotes: 1
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD

9-95078075-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078075
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078075
    reference: chr 9
allele count: 1
allele frequency: 8.434121080242228e-6
allele num: 118566
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*687C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4534C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*687C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.832C>T
  hgvsp: ENSP00000401177.2:p.Leu278Phe
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.628C>T
  hgvsp: ENSP00000351723.4:p.Leu210Phe
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.832C>T
  hgvsp: ENSP00000412471.2:p.Leu278Phe
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.832C>T
  hgvsp: ENSP00000441140.1:p.Leu278Phe
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.676C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.832C>T
  hgvsp: ENSP00000414112.2:p.Leu278Phe
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.628C>T
  hgvsp: ENSP00000440709.1:p.Leu210Phe
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1124C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.832C>T
  hgvsp: ENSP00000439751.1:p.Leu278Phe
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.832C>T
  hgvsp: ENSP00000441300.1:p.Leu278Phe
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 517
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 251
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36171
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1057
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15806
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2430
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Leu278Phe
num of homozygotes: 0
population: African
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum

9-95078079-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078079
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078079
    reference: chr 9
allele count: 19
allele frequency: 1.59698757711769e-4
allele num: 118974
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.828G>A
  hgvsp: ENST00000535387.1:c.828G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*683G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1120G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.828G>A
  hgvsp: ENST00000433029.2:c.828G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.828G>A
  hgvsp: ENST00000545558.1:c.828G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.828G>A
  hgvsp: ENST00000544867.1:c.828G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.624G>A
  hgvsp: ENST00000358855.4:c.624G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.672G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.624G>A
  hgvsp: ENST00000542053.1:c.624G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.828G>A
  hgvsp: ENST00000432670.2:c.828G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4538G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*683G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.828G>A
  hgvsp: ENST00000442668.2:c.828G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 434
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16028
  bin: 2.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 524
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 792
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2428
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 854
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36680
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln276Gln
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ

9-95078087-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078087
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078087
    reference: chr 9
allele count: 4
allele frequency: 3.341240936883959e-5
allele num: 119716
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.820G>A
  hgvsp: ENSP00000441300.1:p.Asp274Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*675G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1112G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.820G>A
  hgvsp: ENSP00000441140.1:p.Asp274Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.820G>A
  hgvsp: ENSP00000412471.2:p.Asp274Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4546G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.820G>A
  hgvsp: ENSP00000439751.1:p.Asp274Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.616G>A
  hgvsp: ENSP00000351723.4:p.Asp206Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.616G>A
  hgvsp: ENSP00000440709.1:p.Asp206Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.820G>A
  hgvsp: ENSP00000414112.2:p.Asp274Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*675G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.820G>A
  hgvsp: ENSP00000401177.2:p.Asp274Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.664G>A
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 426
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37134
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16421
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp274Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD

9-95078092-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078092
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078092
    reference: chr 9
allele count: 21
allele frequency: 1.750145845487124e-4
allele num: 119990
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*670T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.815T>C
  hgvsp: ENSP00000412471.2:p.Val272Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.611T>C
  hgvsp: ENSP00000440709.1:p.Val204Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.815T>C
  hgvsp: ENSP00000441140.1:p.Val272Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.815T>C
  hgvsp: ENSP00000414112.2:p.Val272Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4551T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.659T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.815T>C
  hgvsp: ENSP00000441300.1:p.Val272Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1107T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.815T>C
  hgvsp: ENSP00000401177.2:p.Val272Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.611T>C
  hgvsp: ENSP00000351723.4:p.Val204Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*670T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.815T>C
  hgvsp: ENSP00000439751.1:p.Val272Ala
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 37309
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 16541
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 259
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 376
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Val272Ala
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD

http://identifiers.org/exac.variant/9-95078093-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078093
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078093
    reference: chr 9
allele count: 1
allele frequency: 8.330834083108401e-6
allele num: 120036
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*669G>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4552G>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.610G>T
  hgvsp: ENSP00000440709.1:p.Val204Phe
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.814G>T
  hgvsp: ENSP00000441300.1:p.Val272Phe
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.814G>T
  hgvsp: ENSP00000439751.1:p.Val272Phe
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1106G>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.610G>T
  hgvsp: ENSP00000351723.4:p.Val204Phe
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.658G>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.814G>T
  hgvsp: ENSP00000441140.1:p.Val272Phe
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*669G>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.814G>T
  hgvsp: ENSP00000412471.2:p.Val272Phe
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.814G>T
  hgvsp: ENSP00000414112.2:p.Val272Phe
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.814G>T
  hgvsp: ENSP00000401177.2:p.Val272Phe
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37323
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2518
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 528
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 354
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val272Phe
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: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: DP

http://identifiers.org/exac.variant/9-95078099-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078099
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078099
    reference: chr 9
allele count: 1
allele frequency: 8.316561600771776e-6
allele num: 120242
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1100G>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.604G>T
  hgvsp: ENSP00000351723.4:p.Val202Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.652G>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.604G>T
  hgvsp: ENSP00000440709.1:p.Val202Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.808G>T
  hgvsp: ENSP00000441300.1:p.Val270Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*663G>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.808G>T
  hgvsp: ENSP00000401177.2:p.Val270Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*663G>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.808G>T
  hgvsp: ENSP00000441140.1:p.Val270Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.808G>T
  hgvsp: ENSP00000439751.1:p.Val270Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.808G>T
  hgvsp: ENSP00000414112.2:p.Val270Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4558G>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.808G>T
  hgvsp: ENSP00000412471.2:p.Val270Leu
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2540
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 250
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16699
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Val270Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
reference allele: C
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

http://identifiers.org/exac.variant/9-95078100-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078100
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078100
    reference: chr 9
allele count: 3
allele frequency: 2.494180246092451e-5
allele num: 120280
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1099T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.807T>G
  hgvsp: ENST00000442668.2:c.807T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.807T>G
  hgvsp: ENST00000433029.2:c.807T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.807T>G
  hgvsp: ENST00000544867.1:c.807T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.603T>G
  hgvsp: ENST00000542053.1:c.603T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.651T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.807T>G
  hgvsp: ENST00000535387.1:c.807T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.807T>G
  hgvsp: ENST00000545558.1:c.807T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.807T>G
  hgvsp: ENST00000432670.2:c.807T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*662T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.603T>G
  hgvsp: ENST00000358855.4:c.603T>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*662T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4559T>G
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16732
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro269Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-95078100-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078100
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078100
    reference: chr 9
allele count: 3
allele frequency: 2.494180246092451e-5
allele num: 120280
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*662T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.807T>C
  hgvsp: ENST00000545558.1:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.603T>C
  hgvsp: ENST00000358855.4:c.603T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.807T>C
  hgvsp: ENST00000442668.2:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.807T>C
  hgvsp: ENST00000432670.2:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1099T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.807T>C
  hgvsp: ENST00000544867.1:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.807T>C
  hgvsp: ENST00000433029.2:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.651T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4559T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.603T>C
  hgvsp: ENST00000542053.1:c.603T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*662T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.807T>C
  hgvsp: ENST00000535387.1:c.807T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro269Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: African
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQ

9-95078100-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078100
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078100
    reference: chr 9
allele count: 1
allele frequency: 8.313934153641504e-6
allele num: 120280
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*662T>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.807T>A
  hgvsp: ENST00000535387.1:c.807T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4559T>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.807T>A
  hgvsp: ENST00000442668.2:c.807T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.807T>A
  hgvsp: ENST00000432670.2:c.807T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.807T>A
  hgvsp: ENST00000433029.2:c.807T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*662T>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.603T>A
  hgvsp: ENST00000358855.4:c.603T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.807T>A
  hgvsp: ENST00000545558.1:c.807T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.807T>A
  hgvsp: ENST00000544867.1:c.807T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.651T>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.603T>A
  hgvsp: ENST00000542053.1:c.603T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1099T>A
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2532
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37348
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 151
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 254
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16732
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro269Pro
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

9-95078111-TAGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078111
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078108
    reference: chr 9
allele count: 2
allele frequency: 1.660522732556209e-5
allele num: 120444
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.793_795delTCT
  hgvsp: ENSP00000441140.1:p.Ser265del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.793_795delTCT
  hgvsp: ENSP00000439751.1:p.Ser265del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.793_795delTCT
  hgvsp: ENSP00000441300.1:p.Ser265del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*648_*650delTCT
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.589_591delTCT
  hgvsp: ENSP00000351723.4:p.Ser197del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.793_795delTCT
  hgvsp: ENSP00000412471.2:p.Ser265del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.793_795delTCT
  hgvsp: ENSP00000414112.2:p.Ser265del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*648_*650delTCT
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1085_*1087delTCT
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.589_591delTCT
  hgvsp: ENSP00000440709.1:p.Ser197del
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4573_282-4571delTCT
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.637_639delTCT
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.793_795delTCT
  hgvsp: ENSP00000401177.2:p.Ser265del
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37353
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 525
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16868
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ser265del
num of homozygotes: 0
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
population: Latino
population: East Asian
reference allele: TAGA
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-95078123-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078123
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078123
    reference: chr 9
allele count: 10
allele frequency: 8.296964970213896e-5
allele num: 120526
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*639A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.784A>C
  hgvsp: ENSP00000412471.2:p.Ile262Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.784A>C
  hgvsp: ENSP00000441140.1:p.Ile262Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.784A>C
  hgvsp: ENSP00000414112.2:p.Ile262Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.580A>C
  hgvsp: ENSP00000351723.4:p.Ile194Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.580A>C
  hgvsp: ENSP00000440709.1:p.Ile194Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1076A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.784A>C
  hgvsp: ENSP00000439751.1:p.Ile262Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.784A>C
  hgvsp: ENSP00000441300.1:p.Ile262Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.628A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*639A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4582A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.784A>C
  hgvsp: ENSP00000401177.2:p.Ile262Leu
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 37309
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2572
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 244
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile262Leu
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: DP

9-95078143-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078143
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078143
    reference: chr 9
allele count: 1
allele frequency: 8.294349888855711e-6
allele num: 120564
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4602A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000390143
  ensembl transcript: ENST00000421075
  gene symbol: NOL8
  hgvsc: ENST00000421075.2:c.764A>C
  hgvsp: ENSP00000390143.2:p.Gln255Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*619A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.764A>C
  hgvsp: ENSP00000412471.2:p.Gln255Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.764A>C
  hgvsp: ENSP00000414112.2:p.Gln255Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1056A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.764A>C
  hgvsp: ENSP00000439751.1:p.Gln255Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.560A>C
  hgvsp: ENSP00000351723.4:p.Gln187Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.764A>C
  hgvsp: ENSP00000401177.2:p.Gln255Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.764A>C
  hgvsp: ENSP00000441300.1:p.Gln255Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.560A>C
  hgvsp: ENSP00000440709.1:p.Gln187Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*619A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.764A>C
  hgvsp: ENSP00000441140.1:p.Gln255Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.608A>C
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2596
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17056
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 527
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 153
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln255Pro
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: Other
reference allele: T
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

9-95078145-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078145
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078145
    reference: chr 9
allele count: 9
allele frequency: 7.465162574651626e-5
allele num: 120560
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.762A>T
  hgvsp: ENST00000544867.1:c.762A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.558A>T
  hgvsp: ENST00000542053.1:c.558A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*617A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.762A>T
  hgvsp: ENST00000442668.2:c.762A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.558A>T
  hgvsp: ENST00000358855.4:c.558A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.762A>T
  hgvsp: ENST00000535387.1:c.762A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.762A>T
  hgvsp: ENST00000433029.2:c.762A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.606A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000390143
  ensembl transcript: ENST00000421075
  gene symbol: NOL8
  hgvsc: ENST00000421075.2:c.762A>T
  hgvsp: ENST00000421075.2:c.762A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.762A>T
  hgvsp: ENST00000432670.2:c.762A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4604A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.762A>T
  hgvsp: ENST00000545558.1:c.762A>T(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*617A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1054A>T
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37149
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17070
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
hgvs: p.Ala254Ala
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: QD

9-95078150-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078150
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078150
    reference: chr 9
allele count: 1
allele frequency: 8.2936619835122e-6
allele num: 120574
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.757G>C
  hgvsp: ENSP00000412471.2:p.Ala253Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.757G>C
  hgvsp: ENSP00000439751.1:p.Ala253Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.757G>C
  hgvsp: ENSP00000441300.1:p.Ala253Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.757G>C
  hgvsp: ENSP00000414112.2:p.Ala253Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*612G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000390143
  ensembl transcript: ENST00000421075
  gene symbol: NOL8
  hgvsc: ENST00000421075.2:c.757G>C
  hgvsp: ENSP00000390143.2:p.Ala253Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.553G>C
  hgvsp: ENSP00000351723.4:p.Ala185Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4609G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.757G>C
  hgvsp: ENSP00000401177.2:p.Ala253Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.553G>C
  hgvsp: ENSP00000440709.1:p.Ala185Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.601G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.757G>C
  hgvsp: ENSP00000441140.1:p.Ala253Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*612G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1049G>C
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17111
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 336
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ala253Pro
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum

9-95078167-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078167
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078167
    reference: chr 9
allele count: 1
allele frequency: 8.292148993333113e-6
allele num: 120596
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.740C>G
  hgvsp: ENSP00000441300.1:p.Pro247Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000390143
  ensembl transcript: ENST00000421075
  gene symbol: NOL8
  hgvsc: ENST00000421075.2:c.740C>G
  hgvsp: ENSP00000390143.2:p.Pro247Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.536C>G
  hgvsp: ENSP00000440709.1:p.Pro179Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.584C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.740C>G
  hgvsp: ENSP00000441140.1:p.Pro247Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.740C>G
  hgvsp: ENSP00000414112.2:p.Pro247Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1032C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*595C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.740C>G
  hgvsp: ENSP00000412471.2:p.Pro247Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*595C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.740C>G
  hgvsp: ENSP00000439751.1:p.Pro247Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.536C>G
  hgvsp: ENSP00000351723.4:p.Pro179Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.740C>G
  hgvsp: ENSP00000401177.2:p.Pro247Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4626C>G
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 148
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 531
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2590
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17141
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 145
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37122
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Pro247Arg
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQ

9-95078176-T-TCTATTA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078176
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078182
    reference: chr 9
allele count: 29
allele frequency: 2.404444075947268e-4
allele num: 120610
alternate allele: TCTATTA
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.725_730dupTAATAG
  hgvsp: ENSP00000401177.2:p.Val242_Ile243dup
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.521_526dupTAATAG
  hgvsp: ENSP00000351723.4:p.Val174_Ile175dup
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000390143
  ensembl transcript: ENST00000421075
  gene symbol: NOL8
  hgvsc: ENST00000421075.2:c.725_730dupTAATAG
  hgvsp: ENSP00000390143.2:p.Val242_Ile243dup
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.725_730dupTAATAG
  hgvsp: ENSP00000439751.1:p.Val242_Ile243dup
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.725_730dupTAATAG
  hgvsp: ENSP00000414112.2:p.Val242_Ile243dup
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.725_730dupTAATAG
  hgvsp: ENSP00000412471.2:p.Val242_Ile243dup
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.521_526dupTAATAG
  hgvsp: ENSP00000440709.1:p.Val174_Ile175dup
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: inframe_insertion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.725_730dupTAATAG
  hgvsp: ENSP00000441300.1:p.Val242_Ile243dup
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.569_574dupTAATAG
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*580_*585dupTAATAG
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: inframe_insertion
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.725_730dupTAATAG
  hgvsp: ENSP00000441140.1:p.Val242_Ile243dup
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*580_*585dupTAATAG
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: inframe insertion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 5.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37031
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17172
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 4.75e1
  variant carriers: 7
genotype quality: GenotypeQuality
hgvs: p.Val242_Ile243dup
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum

9-95078179-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078179
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078179
    reference: chr 9
allele count: 16
allele frequency: 1.326545840449699e-4
allele num: 120614
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.572T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.728T>C
  hgvsp: ENSP00000401177.2:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.524T>C
  hgvsp: ENSP00000351723.4:p.Ile175Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.728T>C
  hgvsp: ENSP00000412471.2:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000390143
  ensembl transcript: ENST00000421075
  gene symbol: NOL8
  hgvsc: ENST00000421075.2:c.728T>C
  hgvsp: ENSP00000390143.2:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1020T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*583T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.728T>C
  hgvsp: ENSP00000414112.2:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.728T>C
  hgvsp: ENSP00000439751.1:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.728T>C
  hgvsp: ENSP00000441300.1:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.524T>C
  hgvsp: ENSP00000440709.1:p.Ile175Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*583T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4638T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.728T>C
  hgvsp: ENSP00000441140.1:p.Ile243Thr
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17197
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 530
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 248
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2597
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 37021
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Ile243Thr
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff

9-95078193-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078193
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078193
    reference: chr 9
allele count: 1
allele frequency: 8.290774026663129e-6
allele num: 120616
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*569G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000390143
  ensembl transcript: ENST00000421075
  gene symbol: NOL8
  hgvsc: ENST00000421075.2:c.714G>C
  hgvsp: ENSP00000390143.2:p.Arg238Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.714G>C
  hgvsp: ENSP00000401177.2:p.Arg238Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.558G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.714G>C
  hgvsp: ENSP00000441140.1:p.Arg238Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.714G>C
  hgvsp: ENSP00000439751.1:p.Arg238Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4652G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.510G>C
  hgvsp: ENSP00000440709.1:p.Arg170Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.510G>C
  hgvsp: ENSP00000351723.4:p.Arg170Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.714G>C
  hgvsp: ENSP00000412471.2:p.Arg238Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.714G>C
  hgvsp: ENSP00000441300.1:p.Arg238Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.714G>C
  hgvsp: ENSP00000414112.2:p.Arg238Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*1006G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*569G>C
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2603
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17334
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 36861
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Arg238Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-95078215-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078215
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078215
    reference: chr 9
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*547G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4674G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.692G>A
  hgvsp: ENSP00000441300.1:p.Gly231Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.692G>A
  hgvsp: ENSP00000401177.2:p.Gly231Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000390143
  ensembl transcript: ENST00000421075
  gene symbol: NOL8
  hgvsc: ENST00000421075.2:c.692G>A
  hgvsp: ENSP00000390143.2:p.Gly231Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.692G>A
  hgvsp: ENSP00000441140.1:p.Gly231Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.488G>A
  hgvsp: ENSP00000440709.1:p.Gly163Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.692G>A
  hgvsp: ENSP00000412471.2:p.Gly231Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*984G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.692G>A
  hgvsp: ENSP00000414112.2:p.Gly231Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.692G>A
  hgvsp: ENSP00000439751.1:p.Gly231Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.488G>A
  hgvsp: ENSP00000351723.4:p.Gly163Glu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.536G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*547G>A
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 36387
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2627
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 230
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gly231Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD

9-95078228-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078228
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078228
    reference: chr 9
allele count: 2
allele frequency: 1.658374792703151e-5
allele num: 120600
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.679G>C
  hgvsp: ENSP00000441300.1:p.Glu227Gln
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.679G>C
  hgvsp: ENSP00000439751.1:p.Glu227Gln
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.679G>C
  hgvsp: ENSP00000414112.2:p.Glu227Gln
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.679G>C
  hgvsp: ENSP00000401177.2:p.Glu227Gln
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000390143
  ensembl transcript: ENST00000421075
  gene symbol: NOL8
  hgvsc: ENST00000421075.2:c.679G>C
  hgvsp: ENSP00000390143.2:p.Glu227Gln
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*971G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.475G>C
  hgvsp: ENSP00000351723.4:p.Glu159Gln
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.679G>C
  hgvsp: ENSP00000441140.1:p.Glu227Gln
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.679G>C
  hgvsp: ENSP00000412471.2:p.Glu227Gln
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4687G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.475G>C
  hgvsp: ENSP00000440709.1:p.Glu159Gln
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*534G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.523G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*534G>C
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 536
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 618
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35993
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17631
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 243
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Glu227Gln
num of homozygotes: 0
population: Latino
population: Other
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: MQ

9-95078231-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078231
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078231
    reference: chr 9
allele count: 2
allele frequency: 1.658319790388379e-5
allele num: 120604
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.472G>A
  hgvsp: ENSP00000440709.1:p.Asp158Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.676G>A
  hgvsp: ENSP00000439751.1:p.Asp226Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000390143
  ensembl transcript: ENST00000421075
  gene symbol: NOL8
  hgvsc: ENST00000421075.2:c.676G>A
  hgvsp: ENSP00000390143.2:p.Asp226Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.520G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*531G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.676G>A
  hgvsp: ENSP00000441300.1:p.Asp226Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*968G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*531G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.676G>A
  hgvsp: ENSP00000414112.2:p.Asp226Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.472G>A
  hgvsp: ENSP00000351723.4:p.Asp158Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.676G>A
  hgvsp: ENSP00000401177.2:p.Asp226Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.676G>A
  hgvsp: ENSP00000412471.2:p.Asp226Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.676G>A
  hgvsp: ENSP00000441140.1:p.Asp226Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4690G>A
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 257
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 302
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 289
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2620
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35986
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 242
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Asp226Asn
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ReadPosRankSum

9-95060552-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060552
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060552
    reference: chr 9
allele count: 13
allele frequency: 1.857726714110149e-4
allele num: 69978
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.822C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3295C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3440C>T
  hgvsp: ENSP00000401177.2:p.Thr1147Ile
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3236C>T
  hgvsp: ENSP00000440709.1:p.Thr1079Ile
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3236C>T
  hgvsp: ENSP00000351723.4:p.Thr1079Ile
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3295C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3440C>T
  hgvsp: ENSP00000441140.1:p.Thr1147Ile
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*976C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3326C>T
  hgvsp: ENSP00000441300.1:p.Thr1109Ile
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*970C>T
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1089
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 22802
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3403
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 909
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1213
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 24132
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3640
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 413
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Thr1147Ile
num of homozygotes: 1
population: South Asian
population: African
population: European (Finnish)
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: MQ

9-95060554-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060554
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060554
    reference: chr 9
allele count: 1
allele frequency: 1.404770600960863e-5
allele num: 71186
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3234A>C
  hgvsp: ENST00000358855.4:c.3234A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.820A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3438A>C
  hgvsp: ENST00000545558.1:c.3438A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*968A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3234A>C
  hgvsp: ENST00000542053.1:c.3234A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3293A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*974A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3438A>C
  hgvsp: ENST00000442668.2:c.3438A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3324A>C
  hgvsp: ENST00000535387.1:c.3324A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3293A>C
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23659
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3454
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1044
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3638
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23282
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Thr1146Thr
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: MQ
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD

9-95060555-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060555
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060555
    reference: chr 9
allele count: 1
allele frequency: 1.392563709789723e-5
allele num: 71810
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*967C>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.819C>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3233C>A
  hgvsp: ENSP00000440709.1:p.Thr1078Lys
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3292C>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3437C>A
  hgvsp: ENSP00000401177.2:p.Thr1146Lys
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3292C>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*973C>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3233C>A
  hgvsp: ENSP00000351723.4:p.Thr1078Lys
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3323C>A
  hgvsp: ENSP00000441300.1:p.Thr1108Lys
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3437C>A
  hgvsp: ENSP00000441140.1:p.Thr1146Lys
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23315
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1005
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 914
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1179
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3630
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3498
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1001
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Thr1146Lys
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

9-95060556-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060556
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060556
    reference: chr 9
allele count: 5
allele frequency: 6.911041079228175e-5
allele num: 72348
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3322A>C
  hgvsp: ENSP00000441300.1:p.Thr1108Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3232A>C
  hgvsp: ENSP00000440709.1:p.Thr1078Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3232A>C
  hgvsp: ENSP00000351723.4:p.Thr1078Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3291A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.818A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3291A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3436A>C
  hgvsp: ENSP00000401177.2:p.Thr1146Pro
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*972A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*966A>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3436A>C
  hgvsp: ENSP00000441140.1:p.Thr1146Pro
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 997
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23099
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3623
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 23869
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Thr1146Pro
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
population: African
reference allele: T
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum

9-95060558-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060558
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060558
    reference: chr 9
allele count: 3
allele frequency: 4.097465034965035e-5
allele num: 73216
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3434G>C
  hgvsp: ENSP00000401177.2:p.Arg1145Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*964G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3230G>C
  hgvsp: ENSP00000440709.1:p.Arg1077Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3230G>C
  hgvsp: ENSP00000351723.4:p.Arg1077Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3434G>C
  hgvsp: ENSP00000441140.1:p.Arg1145Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.816G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3320G>C
  hgvsp: ENSP00000441300.1:p.Arg1107Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*970G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3289G>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3289G>C
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3626
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 959
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24206
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3627
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 929
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1232
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22612
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg1145Thr
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: East Asian
reference allele: C
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff

9-95060562-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060562
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060562
    reference: chr 9
allele count: 12
allele frequency: 1.60294942694558e-4
allele num: 74862
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*960G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.812G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3430G>A
  hgvsp: ENSP00000401177.2:p.Ala1144Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3226G>A
  hgvsp: ENSP00000440709.1:p.Ala1076Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3226G>A
  hgvsp: ENSP00000351723.4:p.Ala1076Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3316G>A
  hgvsp: ENSP00000441300.1:p.Ala1106Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3285G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3430G>A
  hgvsp: ENSP00000441140.1:p.Ala1144Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*966G>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3285G>A
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 1.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24550
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 21812
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3870
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 942
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3768
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 903
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala1144Thr
num of homozygotes: 0
population: South Asian
population: East Asian
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: QD

9-95060582-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060582
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060582
    reference: chr 9
allele count: 1
allele frequency: 1.28726636115545e-5
allele num: 77684
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*946T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3410T>C
  hgvsp: ENSP00000441140.1:p.Met1137Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3265T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3206T>C
  hgvsp: ENSP00000351723.4:p.Met1069Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.792T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3296T>C
  hgvsp: ENSP00000441300.1:p.Met1099Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*940T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3206T>C
  hgvsp: ENSP00000440709.1:p.Met1069Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3410T>C
  hgvsp: ENSP00000401177.2:p.Met1137Thr
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3265T>C
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1320
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5364
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20486
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 338
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Met1137Thr
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

9-95060594-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060594
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060594
    reference: chr 9
allele count: 1
allele frequency: 1.336148152107106e-5
allele num: 74842
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3194T>C
  hgvsp: ENSP00000351723.4:p.Val1065Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.780T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3398T>C
  hgvsp: ENSP00000441140.1:p.Val1133Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3253T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*928T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3194T>C
  hgvsp: ENSP00000440709.1:p.Val1065Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3253T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3284T>C
  hgvsp: ENSP00000441300.1:p.Val1095Ala
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*934T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3398T>C
  hgvsp: ENSP00000401177.2:p.Val1133Ala
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1343
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19202
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21414
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1670
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4438
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20443
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Val1133Ala
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: QD
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD

9-95060623-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060623
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060623
    reference: chr 9
allele count: 3
allele frequency: 4.689258471926972e-5
allele num: 63976
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3374-5A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3170-5A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3170-5A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3229-5A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*910-5A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*904-5A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3374-5A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3260-5A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3229-5A>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.751A>T
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23565
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3374-5A>T
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: East Asian
reference allele: T
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

9-95078236-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95078236
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95078236
    reference: chr 9
allele count: 1
allele frequency: 8.2917364554485e-6
allele num: 120602
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*526A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000390143
  ensembl transcript: ENST00000421075
  gene symbol: NOL8
  hgvsc: ENST00000421075.2:c.671A>G
  hgvsp: ENSP00000390143.2:p.Gln224Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000414112
  ensembl transcript: ENST00000432670
  gene symbol: NOL8
  hgvsc: ENST00000432670.2:c.671A>G
  hgvsp: ENSP00000414112.2:p.Gln224Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.671A>G
  hgvsp: ENSP00000441140.1:p.Gln224Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000412471
  ensembl transcript: ENST00000433029
  gene symbol: NOL8
  hgvsc: ENST00000433029.2:c.671A>G
  hgvsp: ENSP00000412471.2:p.Gln224Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*526A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000467230
  gene symbol: NOL8
  hgvsc: ENST00000467230.1:n.515A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.282-4695A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000415750
  ensembl transcript: ENST00000434228
  gene symbol: NOL8
  hgvsc: ENST00000434228.1:c.*963A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.671A>G
  hgvsp: ENSP00000401177.2:p.Gln224Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.671A>G
  hgvsp: ENSP00000439751.1:p.Gln224Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.671A>G
  hgvsp: ENSP00000441300.1:p.Gln224Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.467A>G
  hgvsp: ENSP00000440709.1:p.Gln156Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.467A>G
  hgvsp: ENSP00000351723.4:p.Gln156Arg
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 179
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 335
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35943
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 245
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: p.Gln224Arg
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD

9-95060623-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060623
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060623
    reference: chr 9
allele count: 1
allele frequency: 1.563086157308991e-5
allele num: 63976
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3170-5A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3374-5A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3260-5A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3374-5A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*910-5A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3229-5A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3170-5A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*904-5A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.751A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3229-5A>G
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2409
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7833
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23565
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15227
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2797
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 136
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3374-5A>G
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: African
population: Other
population: South Asian
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

http://identifiers.org/exac.variant/9-95060624-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060624
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060624
    reference: chr 9
allele count: 1
allele frequency: 1.585137748470342e-5
allele num: 63086
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3374-6T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*910-6T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3170-6T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.750T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3229-6T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3170-6T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3260-6T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3229-6T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*904-6T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3374-6T>G
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 23469
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 339
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2450
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4820
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7364
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 15468
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3374-6T>G
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: A
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum

9-95060628-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060628
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060628
    reference: chr 9
allele count: 2
allele frequency: 3.335445782328808e-5
allele num: 59962
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3374-10C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3229-10C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.746C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*904-10C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3170-10C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*910-10C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3170-10C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3229-10C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3374-10C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3260-10C>T
  variant of: http://identifiers.org/hgnc/23387
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 135
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23279
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6157
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2567
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5923
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15883
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 105
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1072
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 268
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2746
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 273
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1382
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: G
site quality: DP
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

9-95060630-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060630
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060630
    reference: chr 9
allele count: 3450
allele frequency: 5.669679539852095e-2
allele num: 60850
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3229-12T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*910-12T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3374-12T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3229-12T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3260-12T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.744T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3374-12T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3170-12T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*904-12T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3170-12T>C
  variant of: http://identifiers.org/hgnc/23387
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 6.25e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 16065
  bin: 1.25e1
  variant carriers: 1279
genotype depth: GenotypeDepth
  all individuals: 5614
  bin: 2.25e1
  variant carriers: 348
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 7.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 2406
  bin: 1.75e1
  variant carriers: 769
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 5.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 1094
  bin: 9.75e1
  variant carriers: 129
genotype depth: GenotypeDepth
  all individuals: 499
  bin: 3.75e1
  variant carriers: 127
genotype depth: GenotypeDepth
  all individuals: 6116
  bin: 2.5e0
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 23146
  bin: 7.5e0
  variant carriers: 770
genotype depth: GenotypeDepth
  all individuals: 2489
  bin: 2.75e1
  variant carriers: 221
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 4.75e1
  variant carriers: 59
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 8.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 7.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 8.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 907
  bin: 3.25e1
  variant carriers: 182
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.25e1
  variant carriers: 103
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 5.25e1
  variant carriers: 34
genotype quality: GenotypeQuality
  all individuals: 763
  bin: 6.75e1
  variant carriers: 32
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 7.75e1
  variant carriers: 50
genotype quality: GenotypeQuality
  all individuals: 6571
  bin: 6.25e1
  variant carriers: 45
num of homozygotes: 103
population: Other
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: A
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

9-95060640-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060640
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060640
    reference: chr 9
allele count: 1
allele frequency: 1.886650064146102e-5
allele num: 53004
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3374-22T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3170-22T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*910-22T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3170-22T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3229-22T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3229-22T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.734T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3260-22T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3374-22T>C
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*904-22T>C
  variant of: http://identifiers.org/hgnc/23387
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 402
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2175
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2037
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2756
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: African
population: European (Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS

9-95060644-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060644
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060644
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 50656
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.730C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3170-26C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3374-26C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3260-26C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3170-26C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3229-26C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*904-26C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3229-26C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3374-26C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*910-26C>T
  variant of: http://identifiers.org/hgnc/23387
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 11191
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 345
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23089
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14446
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3176
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 398
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11851
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2365
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2777
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: European (Finnish)
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/9-95060657-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060657
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060657
    reference: chr 9
allele count: 1
allele frequency: 2.437122246051862e-5
allele num: 41032
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3170-39T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3260-39T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.717T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3229-39T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3170-39T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3374-39T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*904-39T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3374-39T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3229-39T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*910-39T>G
  variant of: http://identifiers.org/hgnc/23387
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 341
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10396
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 386
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13557
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1244
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2081
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14692
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 584
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1178
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum

9-95060667-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95060667
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95060667
    reference: chr 9
allele count: 1
allele frequency: 2.743484224965706e-5
allele num: 36450
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3170-49A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3260-49A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*910-49A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*904-49A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3170-49A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3374-49A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3374-49A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3229-49A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.707A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3229-49A>G
  variant of: http://identifiers.org/hgnc/23387
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13728
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26733
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8743
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3274
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 380
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2464
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

9-95061133-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95061133
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95061133
    reference: chr 9
allele count: 1231
allele frequency: 5.86469747498809e-2
allele num: 20990
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3373+33T>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.241T>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3259+33T>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3228+33T>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*903+33T>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3169+33T>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*909+33T>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3373+33T>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3169+33T>A
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3228+33T>A
  variant of: http://identifiers.org/hgnc/23387
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 4.25e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 7.5e0
  variant carriers: 526
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2180
  bin: 1.25e1
  variant carriers: 241
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 758
  bin: 3.25e1
  variant carriers: 40
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 5.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 1158
  bin: 1.75e1
  variant carriers: 263
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2426
  bin: 2.25e1
  variant carriers: 212
genotype depth: GenotypeDepth
  all individuals: 33374
  bin: 2.5e0
  variant carriers: 271
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 5.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 3.75e1
  variant carriers: 31
genotype depth: GenotypeDepth
  all individuals: 643
  bin: 9.75e1
  variant carriers: 147
genotype depth: GenotypeDepth
  all individuals: 255
  bin: 4.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 8.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 2.75e1
  variant carriers: 92
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 4.25e1
  variant carriers: 15
genotype quality: GenotypeQuality
  all individuals: 192
  bin: 5.25e1
  variant carriers: 46
genotype quality: GenotypeQuality
  all individuals: 2008
  bin: 1.25e1
  variant carriers: 60
num of homozygotes: 47
population: African
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

9-95061138-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95061138
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95061138
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 21054
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3373+28A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*909+28A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3373+28A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3228+28A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3169+28A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3228+28A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*903+28A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.236A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3259+28A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3169+28A>G
  variant of: http://identifiers.org/hgnc/23387
canonical: false
consequence: non coding transcript exon
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6642
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1944
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34337
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2892
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1528
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 940
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1966
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 256
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum

http://identifiers.org/exac.variant/9-95061185-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95061185
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95061185
    reference: chr 9
allele count: 2
allele frequency: 8.86053517632465e-5
allele num: 22572
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3150G>T
  hgvsp: ENSP00000440709.1:p.Lys1050Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3354G>T
  hgvsp: ENSP00000401177.2:p.Lys1118Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*890G>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*884G>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3240G>T
  hgvsp: ENSP00000441300.1:p.Lys1080Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3150G>T
  hgvsp: ENSP00000351723.4:p.Lys1050Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3354G>T
  hgvsp: ENSP00000441140.1:p.Lys1118Asn
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3209G>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.189G>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3209G>T
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10093
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32667
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2265
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5215
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 855
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 417
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 253
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Lys1118Asn
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: African
population: European (Finnish)
population: South Asian
reference allele: C
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: DP

9-95061207-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95061207
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95061207
    reference: chr 9
allele count: 6
allele frequency: 2.664535038635758e-4
allele num: 22518
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*862C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3128C>G
  hgvsp: ENSP00000351723.4:p.Thr1043Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3187C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3128C>G
  hgvsp: ENSP00000440709.1:p.Thr1043Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*868C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3187C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3332C>G
  hgvsp: ENSP00000401177.2:p.Thr1111Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3218C>G
  hgvsp: ENSP00000441300.1:p.Thr1073Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3332C>G
  hgvsp: ENSP00000441140.1:p.Thr1111Ser
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.167C>G
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2285
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8474
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 409
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 400
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 857
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5191
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31396
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr1111Ser
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: South Asian
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

9-95061209-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95061209
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95061209
    reference: chr 9
allele count: 1
allele frequency: 4.448002846721822e-5
allele num: 22482
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3185C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3330C>G
  hgvsp: ENST00000442668.2:c.3330C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3216C>G
  hgvsp: ENST00000535387.1:c.3216C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*866C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3330C>G
  hgvsp: ENST00000545558.1:c.3330C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3126C>G
  hgvsp: ENST00000542053.1:c.3126C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3126C>G
  hgvsp: ENST00000358855.4:c.3126C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*860C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.165C>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3185C>G
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33259
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5182
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 858
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8249
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 408
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2282
  bin: 2.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2051
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Thr1110Thr
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: South Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD

9-95061216-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95061216
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95061216
    reference: chr 9
allele count: 1
allele frequency: 4.458314757021846e-5
allele num: 22430
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.158A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3323A>G
  hgvsp: ENSP00000401177.2:p.Lys1108Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3178A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*853A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*859A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3178A>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3119A>G
  hgvsp: ENSP00000351723.4:p.Lys1040Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3119A>G
  hgvsp: ENSP00000440709.1:p.Lys1040Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3209A>G
  hgvsp: ENSP00000441300.1:p.Lys1070Arg
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3323A>G
  hgvsp: ENSP00000441140.1:p.Lys1108Arg
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 421
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7388
  bin: 7.5e0
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2299
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33548
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5123
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 833
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31721
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Lys1108Arg
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum

9-95061228-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95061228
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95061228
    reference: chr 9
allele count: 0
allele frequency: 0.0e0
allele num: 22208
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.146C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3166C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*841C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3107C>T
  hgvsp: ENSP00000351723.4:p.Ser1036Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3107C>T
  hgvsp: ENSP00000440709.1:p.Ser1036Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3197C>T
  hgvsp: ENSP00000441300.1:p.Ser1066Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3166C>T
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3311C>T
  hgvsp: ENSP00000401177.2:p.Ser1104Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3311C>T
  hgvsp: ENSP00000441140.1:p.Ser1104Leu
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*847C>T
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: missense
filter: AC_Adj0_Filter
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5947
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2298
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 537
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 811
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33780
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 826
  bin: 6.75e1
  variant carriers: 1
hgvs: p.Ser1104Leu
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/9-95061243-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 95061243
    reference: chr 9
  end: Position
    type: ExactPosition
    position: 95061243
    reference: chr 9
allele count: 6
allele frequency: 2.752546105147261e-4
allele num: 21798
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439751
  ensembl transcript: ENST00000544867
  gene symbol: NOL8
  hgvsc: ENST00000544867.1:c.*839-7T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000440709
  ensembl transcript: ENST00000542053
  gene symbol: NOL8
  hgvsc: ENST00000542053.1:c.3099-7T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441140
  ensembl transcript: ENST00000545558
  gene symbol: NOL8
  hgvsc: ENST00000545558.1:c.3303-7T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000401177
  ensembl transcript: ENST00000442668
  gene symbol: NOL8
  hgvsc: ENST00000442668.2:c.3303-7T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl transcript: ENST00000463593
  gene symbol: NOL8
  hgvsc: ENST00000463593.2:n.138-7T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000354115
  ensembl transcript: ENST00000360868
  gene symbol: NOL8
  hgvsc: ENST00000360868.3:c.*3158-7T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000441300
  ensembl transcript: ENST00000535387
  gene symbol: NOL8
  hgvsc: ENST00000535387.1:c.3189-7T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000351723
  ensembl transcript: ENST00000358855
  gene symbol: NOL8
  hgvsc: ENST00000358855.4:c.3099-7T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000439829
  ensembl transcript: ENST00000545444
  gene symbol: NOL8
  hgvsc: ENST00000545444.1:c.*833-7T>G
  variant of: http://identifiers.org/hgnc/23387
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000198000
  ensembl protein: ENSP00000446265
  ensembl transcript: ENST00000536593
  gene symbol: NOL8
  hgvsc: ENST00000536593.1:c.*3158-7T>G
  variant of: http://identifiers.org/hgnc/23387
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4089
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2150
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 767
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 252
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 529
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32957
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1215
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4055
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
hgvs: c.3303-7T>G
num of homozygotes: 0
reference allele: A

GenotypeDepth
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 9726
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4197
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 157
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 300
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1572
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2525
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 2364
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 290
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3810
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3266
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 526
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 607
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1924
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7839
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1125
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 477
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4485
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28443
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9280
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7910
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 3.878975950349108e-4
allele num: 15468
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.628028132326127e-5
allele num: 61424
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6360
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10380
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

QD
type: SiteQuality
SIO_000300: 1.465e1

MQ
type: SiteQuality
SIO_000300: 5.658e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 3.09e0

MQRankSum
type: SiteQuality
SIO_000300: -1.116e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.7e-2

DP
type: SiteQuality
SIO_000300: 1.319738e6

FS
type: SiteQuality
SIO_000300: 4.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.67e-1

GenotypeDepth
all individuals: 8594
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 9902
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4460
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 28572
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3265
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 306
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 283
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1192
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 7835
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 436
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2355
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1544
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1887
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3784
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 603
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2520
bin: 9.75e1
variant carriers: 2

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 61432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7914
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9276
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6356
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 850
num of homozygotes: 0

South Asian
type: Population
allele count: 2
allele frequency: 1.292657704239917e-4
allele num: 15472
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.028e0

ClippingRankSum
type: SiteQuality
SIO_000300: 9.83e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.44e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.79e0

DP
type: SiteQuality
SIO_000300: 1.320406e6

MQRankSum
type: SiteQuality
SIO_000300: 2.34e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 4145
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1830
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4231
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1411
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3372
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 620
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1691
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3106
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 7606
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 516
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1315
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29730
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 316
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 538
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2372
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2520
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 281
bin: 7.5e0
variant carriers: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9280
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15496
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7906
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.626598132665344e-5
allele num: 61478
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -5.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.09e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.111e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.367e0

FS
type: SiteQuality
SIO_000300: 8.45e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.23e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.61e0

DP
type: SiteQuality
SIO_000300: 1.33046e6

GenotypeDepth
all individuals: 1870
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 6154
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 332
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 113
bin: 8.75e1
variant carriers: 1

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 177
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1320
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2525
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 1844
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 115
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 210
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3631
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1079
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2475
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1428
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6931
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31373
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2680
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2698
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 561
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9314
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6396
num of homozygotes: 0

South Asian
type: Population
allele count: 4
allele frequency: 2.570363706464465e-4
allele num: 15562
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7962
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.616814874696847e-5
allele num: 61850
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -2.83e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-3

DP
type: SiteQuality
SIO_000300: 1.355286e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e0

VQSLOD
type: SiteQuality
SIO_000300: 7.8e-1

QD
type: SiteQuality
SIO_000300: 1.275e1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.41e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.16e-1

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 7844
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2504
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1197
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6684
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2523
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3367
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2457
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34016
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2515
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7958
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.612903225806452e-5
allele num: 62000
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10522
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9334
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15598
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 1.053e1

FS
type: SiteQuality
SIO_000300: 1.674e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

DP
type: SiteQuality
SIO_000300: 1.365762e6

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

GenotypeDepth
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 1902
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 246
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 27225
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 330
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1264
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 966
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34016
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 100
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1197
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2523
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6684
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2457
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2515
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3367
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 662
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2504
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62000
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7958
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 858
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15598
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9334
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.8e0

DP
type: SiteQuality
SIO_000300: 1.365762e6

ClippingRankSum
type: SiteQuality
SIO_000300: -9.370000000000001e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 1.674e0

MQRankSum
type: SiteQuality
SIO_000300: -5.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

QD
type: SiteQuality
SIO_000300: 1.053e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 3.28e0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 5390
bin: 1.75e1
variant carriers: 1

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 332
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2521
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2450
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1229
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3283
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34321
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6578
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 569
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2358
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 931
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 98
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 571
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1258
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 665
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2545
bin: 6.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 862
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9336
num of homozygotes: 0

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

Latino
type: Population
allele count: 1
allele frequency: 9.487666034155598e-5
allele num: 10540
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7966
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6412
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62046
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 2.003e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

VQSLOD
type: SiteQuality
SIO_000300: -8.840000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.25e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.43e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.25e-1

DP
type: SiteQuality
SIO_000300: 1.369251e6

BaseQRankSum
type: SiteQuality
SIO_000300: -6.34e-1

QD
type: SiteQuality
SIO_000300: 7.81e0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 512
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 330
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 669
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1549
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3217
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2522
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 328
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2419
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 975
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 170
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6458
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 93
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 180
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33806
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2554
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1293
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 911
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 581
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.609372988283765e-5
allele num: 62136
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15634
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9348
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6416
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 866
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7980
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -3.393e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.095e0

MQRankSum
type: SiteQuality
SIO_000300: 1.3e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.642e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.96e-1

DP
type: SiteQuality
SIO_000300: 1.372515e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.992e1

GenotypeDepth
all individuals: 254
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1169
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3026
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 326
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2522
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 35083
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6252
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2278
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 685
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 578
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2604
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2184
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1247
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 848
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7998
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15648
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.60621928105625e-5
allele num: 62258
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9354
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

QD
type: SiteQuality
SIO_000300: 2.023e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.46e0

DP
type: SiteQuality
SIO_000300: 1.380214e6

ClippingRankSum
type: SiteQuality
SIO_000300: 7.92e-1

MQRankSum
type: SiteQuality
SIO_000300: 6.34e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: -1.636e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.38e-1

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 246
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2001
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 256
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 125
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1216
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 596
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2522
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 37136
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1856
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2590
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1147
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5633
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2665
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 789
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.356470887363335e-5
allele num: 15732
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62596
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10646
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9390
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8036
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.1e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.45e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.923e1

QD
type: SiteQuality
SIO_000300: 9.289999999999999e0

VQSLOD
type: SiteQuality
SIO_000300: 6.4e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -5.29e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.72e-1

DP
type: SiteQuality
SIO_000300: 1.40117e6

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 518
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 3252
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 1997
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1803
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2485
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5478
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 794
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1159
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1927
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 693
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1265
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2716
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37462
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 504
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2525
bin: 9.75e1
variant carriers: 5

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8050
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6446
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 7.972192990847923e-5
allele num: 62718
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9394
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10684
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 3.29e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.46e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.14e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.57e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.06e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.09e-1

DP
type: SiteQuality
SIO_000300: 1.405622e6

QD
type: SiteQuality
SIO_000300: 1.338e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 330
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2043
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 246
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 612
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2523
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 5060
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1754
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2783
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2177
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1681
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 385
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 692
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1154
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 38795
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 334
bin: 8.25e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62956
num of homozygotes: 0

East Asian
type: Population
allele count: 3
allele frequency: 3.713790542213419e-4
allele num: 8078
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10752
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15824
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6462
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.74e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.420467e6

QD
type: SiteQuality
SIO_000300: 9.52e0

BaseQRankSum
type: SiteQuality
SIO_000300: -8.3e-1

FS
type: SiteQuality
SIO_000300: 7.847e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: 3.05e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.29e-1

GenotypeDepth
all individuals: 331
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 30820
bin: 2.25e1
variant carriers: 1

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 179
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1127
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1722
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5015
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2791
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1635
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39051
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 369
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1018
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2142
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 621
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 342
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 694
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2521
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6464
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10762
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8088
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15832
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.587200812646816e-5
allele num: 63004
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9434
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.929e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.01e-1

QD
type: SiteQuality
SIO_000300: 4.73e0

DP
type: SiteQuality
SIO_000300: 1.422674e6

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

BaseQRankSum
type: SiteQuality
SIO_000300: 5.36e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.438e0

ClippingRankSum
type: SiteQuality
SIO_000300: 7.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

GenotypeDepth
all individuals: 251
bin: 6.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 246
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 551
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2967
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 119
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1274
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 625
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1792
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 148
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 729
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4286
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1486
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1412
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39870
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1210
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2521
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 331
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.576044129235618e-5
allele num: 63450
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8152
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9454
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10882
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.01e0

VQSLOD
type: SiteQuality
SIO_000300: -1.17e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 6.61e0

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.378e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.14e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.37e-1

DP
type: SiteQuality
SIO_000300: 1.445102e6

GenotypeDepth
all individuals: 256
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 31567
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 516
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 722
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4194
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2521
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 40141
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1452
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 713
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 530
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1152
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2953
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 123
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1763
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1273
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1378
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 7.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6488
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15920
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9460
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8162
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 9.184423218221895e-5
allele num: 10888
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.817e0

QD
type: SiteQuality
SIO_000300: 8.19e0

DP
type: SiteQuality
SIO_000300: 1.447434e6

MQ
type: SiteQuality
SIO_000300: 6.107e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.056e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.59e0

FS
type: SiteQuality
SIO_000300: 2.098e0

MQRankSum
type: SiteQuality
SIO_000300: -4.2e-2

GenotypeDepth
all individuals: 13548
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 31891
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 520
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1134
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 72
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1289
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1221
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 96
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2521
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3913
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40908
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 690
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1345
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 327
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 703
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2985
bin: 6.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15950
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10918
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9466
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8184
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.570549063952758e-5
allele num: 63672
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.84e-1

QD
type: SiteQuality
SIO_000300: 2.056e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 7.38e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.623e0

VQSLOD
type: SiteQuality
SIO_000300: -6.382e-1

DP
type: SiteQuality
SIO_000300: 1.457023e6

FS
type: SiteQuality
SIO_000300: 6.029e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 332
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 246
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2522
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1143
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3059
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1435
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 323
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1242
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1238
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41738
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 632
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3606
bin: 2.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8210
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.053740779768177e-4
allele num: 9490
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10992
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 63902
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16012
num of homozygotes: 0

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

QD
type: SiteQuality
SIO_000300: 1.305e1

VQSLOD
type: SiteQuality
SIO_000300: 6.05e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.96e-1

DP
type: SiteQuality
SIO_000300: 1.467318e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.07e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.889999999999999e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

MQ
type: SiteQuality
SIO_000300: 5.945e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.516e0

GenotypeDepth
all individuals: 301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 334
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15161
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2360
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 535
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3255
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 468
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2523
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 60
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 314
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 656
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 758
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45914
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 686
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 797
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 343
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 673
bin: 7.75e1
variant carriers: 0

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

Other
type: Population
allele count: 1
allele frequency: 1.131221719457014e-3
allele num: 884
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9568
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16162
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64770
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11216
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6542
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8310
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -1.789e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.4e0

QD
type: SiteQuality
SIO_000300: 1.646e1

MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 7.075e0

DP
type: SiteQuality
SIO_000300: 1.507791e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.76e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.71e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.75e-1

GenotypeDepth
all individuals: 15229
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 520
bin: 3.75e1
variant carriers: 1

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 246
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 761
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 266
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3328
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2272
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 624
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 770
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46317
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 401
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 640
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 450
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 697
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 347
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2525
bin: 9.75e1
variant carriers: 2

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11240
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9574
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64852
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.402691013935608e-4
allele num: 8324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16178
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.509685e6

VQSLOD
type: SiteQuality
SIO_000300: 9.350000000000001e-1

QD
type: SiteQuality
SIO_000300: 1.334e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.11e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.6e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.11e-1

FS
type: SiteQuality
SIO_000300: 5.403e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.6e-3

GenotypeDepth
all individuals: 252
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 5.75e1
variant carriers: 2

GenotypeDepth
all individuals: 301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 35012
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 15300
bin: 2.75e1
variant carriers: 2

GenotypeQuality
all individuals: 425
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 478
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3340
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 773
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 723
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 601
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 687
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2208
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 258
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46754
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2531
bin: 9.75e1
variant carriers: 8

GenotypeQuality
all individuals: 343
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 2.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11248
num of homozygotes: 0

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

South Asian
type: Population
allele count: 7
allele frequency: 4.323656578134651e-4
allele num: 16190
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64916
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9582
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6546
num of homozygotes: 0

East Asian
type: Population
allele count: 2
allele frequency: 2.400960384153662e-4
allele num: 8330
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 3.263e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.793e0

QD
type: SiteQuality
SIO_000300: 1.453e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.6e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.95e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.25e-1

DP
type: SiteQuality
SIO_000300: 1.512455e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-2

MQ
type: SiteQuality
SIO_000300: 5.946e1

VQSLOD
type: SiteQuality
SIO_000300: 7.13e-1

GenotypeDepth
all individuals: 258
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 317
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2522
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 11
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1529
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 344
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 419
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 48602
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 791
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3454
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 152
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 352
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 705
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9628
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6568
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11324
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16272
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.527277170260859e-5
allele num: 65476
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.21e-1

QD
type: SiteQuality
SIO_000300: 1.262e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.27e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.45e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

FS
type: SiteQuality
SIO_000300: 1.494e0

DP
type: SiteQuality
SIO_000300: 1.531942e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.307e0

MQRankSum
type: SiteQuality
SIO_000300: 6.2e-2

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 301
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 243
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 342
bin: 4.25e1
variant carriers: 2

GenotypeQuality
all individuals: 294
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 104
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 246
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 151
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 221
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 12
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1202
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 220
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49416
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3518
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 182
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 351
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2540
bin: 9.75e1
variant carriers: 19

GenotypeQuality
all individuals: 699
bin: 7.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8442
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65712
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11368
num of homozygotes: 0

South Asian
type: Population
allele count: 19
allele frequency: 1.163502755664421e-3
allele num: 16330
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9658
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.540993e6

QD
type: SiteQuality
SIO_000300: 1.316e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.52e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.8e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.8e-3

MQRankSum
type: SiteQuality
SIO_000300: -7.89e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.146e0

VQSLOD
type: SiteQuality
SIO_000300: -9.866e-1

FS
type: SiteQuality
SIO_000300: 5.47e-1

MQ
type: SiteQuality
SIO_000300: 5.689e1

GenotypeDepth
all individuals: 529
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 59
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50457
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 717
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 129
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 704
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 122
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2526
bin: 9.75e1
variant carriers: 4

GenotypeQuality
all individuals: 144
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 116
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 824
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3595
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16390
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.044122091266244e-5
allele num: 66180
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9704
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -8.78e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.594e0

MQRankSum
type: SiteQuality
SIO_000300: 1.59e0

QD
type: SiteQuality
SIO_000300: 1.45e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.34e0

DP
type: SiteQuality
SIO_000300: 1.553476e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.13e-2

FS
type: SiteQuality
SIO_000300: 2.193e0

VQSLOD
type: SiteQuality
SIO_000300: 2.83e-1

GenotypeDepth
all individuals: 2498
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 232
bin: 7.25e1
variant carriers: 2

GenotypeDepth
all individuals: 332
bin: 4.25e1
variant carriers: 0

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

GenotypeDepth
all individuals: 87
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3658
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2541
bin: 9.75e1
variant carriers: 21

GenotypeQuality
all individuals: 186
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 525
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 730
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 364
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50765
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.25e1
variant carriers: 0

African
type: Population
allele count: 20
allele frequency: 2.056766762649116e-3
allele num: 9724
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16424
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66348
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 1
allele frequency: 8.715356458079135e-5
allele num: 11474
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.984e1

DP
type: SiteQuality
SIO_000300: 1.557958e6

QD
type: SiteQuality
SIO_000300: 1.543e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.76e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.3e0

MQRankSum
type: SiteQuality
SIO_000300: 2.27e-1

FS
type: SiteQuality
SIO_000300: 1.174e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.67e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.99e0

GenotypeDepth
all individuals: 302
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 244
bin: 5.25e1
variant carriers: 1

GenotypeDepth
all individuals: 332
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 177
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 71
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2523
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3656
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 837
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 501
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50830
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66374
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6586
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.027960526315789e-4
allele num: 9728
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.86e-1

VQSLOD
type: SiteQuality
SIO_000300: -9.587e-1

QD
type: SiteQuality
SIO_000300: 1.16e0

FS
type: SiteQuality
SIO_000300: 1.532e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.112e0

DP
type: SiteQuality
SIO_000300: 1.558046e6

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

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 252
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 302
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 528
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 243
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 67
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2523
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 58
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 362
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3690
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51025
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 847
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 164
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16464
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11498
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504619180885318e-5
allele num: 66462
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8576
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.689e0

DP
type: SiteQuality
SIO_000300: 1.56148e6

MQRankSum
type: SiteQuality
SIO_000300: 7.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.34e0

VQSLOD
type: SiteQuality
SIO_000300: 3.15e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.3e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.184e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.753e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.51e-1

GenotypeDepth
all individuals: 2532
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37348
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 302
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3702
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51064
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 853
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2529
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.512771142332802e-5
allele num: 66478
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 2.13e-1

QD
type: SiteQuality
SIO_000300: 1.334e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.589e0

DP
type: SiteQuality
SIO_000300: 1.561779e6

VQSLOD
type: SiteQuality
SIO_000300: 2.5e0

FS
type: SiteQuality
SIO_000300: 1.295e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

GenotypeDepth
all individuals: 16732
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

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

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51064
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2529
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 853
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3702
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

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

East Asian
type: Population
allele count: 3
allele frequency: 3.494874184529357e-4
allele num: 8584
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66478
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.295e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.13e-1

QD
type: SiteQuality
SIO_000300: 1.334e1

VQSLOD
type: SiteQuality
SIO_000300: 2.5e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.589e0

DP
type: SiteQuality
SIO_000300: 1.561779e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 525
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 302
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 736
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51064
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3702
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2529
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 78
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 65
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 853
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 8.25e1
variant carriers: 0

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

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.504257047444267e-5
allele num: 66478
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 2.5e0

QD
type: SiteQuality
SIO_000300: 1.334e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.589e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

FS
type: SiteQuality
SIO_000300: 1.295e0

MQRankSum
type: SiteQuality
SIO_000300: 2.13e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.7e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.561779e6

GenotypeDepth
all individuals: 218
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeDepth
all individuals: 332
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2555
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 189
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 859
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 244
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51203
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3733
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2524
bin: 9.75e1
variant carriers: 2

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

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 367
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 7.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9752
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66570
num of homozygotes: 0

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

South Asian
type: Population
allele count: 2
allele frequency: 1.21256214380987e-4
allele num: 16494
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.16e0

FS
type: SiteQuality
SIO_000300: 1.598e0

DP
type: SiteQuality
SIO_000300: 1.564378e6

MQRankSum
type: SiteQuality
SIO_000300: -6.99e-1

QD
type: SiteQuality
SIO_000300: 1.393e1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.23e-1

MQ
type: SiteQuality
SIO_000300: 5.691e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.71e-1

GenotypeDepth
all individuals: 302
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 248
bin: 5.75e1
variant carriers: 1

GenotypeDepth
all individuals: 219
bin: 6.75e1
variant carriers: 2

GenotypeDepth
all individuals: 151
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 16968
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 525
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3751
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 867
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 46
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 61
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 8.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2531
bin: 9.75e1
variant carriers: 10

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

GenotypeQuality
all individuals: 51278
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 734
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

South Asian
type: Population
allele count: 8
allele frequency: 4.847309743092584e-4
allele num: 16504
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.002642325246217e-5
allele num: 66608
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.968e1

FS
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: -9.6e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -8.400000000000001e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.41e0

BaseQRankSum
type: SiteQuality
SIO_000300: 3.26e0

QD
type: SiteQuality
SIO_000300: 1.31e1

DP
type: SiteQuality
SIO_000300: 1.566191e6

GenotypeDepth
all individuals: 37177
bin: 2.25e1
variant carriers: 0

GenotypeDepth
all individuals: 253
bin: 6.25e1
variant carriers: 1

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

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 336
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 257
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 372
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 51154
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 72
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3764
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2523
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500870504892838e-5
allele num: 66628
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9756
num of homozygotes: 0

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

QD
type: SiteQuality
SIO_000300: 1.453e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.21e0

FS
type: SiteQuality
SIO_000300: 2.122e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.85e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.19e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 7.19e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.53e-1

DP
type: SiteQuality
SIO_000300: 1.566874e6

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 303
bin: 9.75e1
variant carriers: 1

GenotypeDepth
all individuals: 157
bin: 8.25e1
variant carriers: 1

GenotypeDepth
all individuals: 529
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 152
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 87
bin: 9.25e1
variant carriers: 1

GenotypeDepth
all individuals: 257
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 65
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 71
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3769
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 95
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 18
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 74
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 874
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 736
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51133
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2531
bin: 9.75e1
variant carriers: 9

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

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

African
type: Population
allele count: 9
allele frequency: 9.226983801517326e-4
allele num: 9754
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66624
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 7.33e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.56e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 2.06e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.600000000000001e-1

DP
type: SiteQuality
SIO_000300: 1.567321e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.29e-1

FS
type: SiteQuality
SIO_000300: 5.22e-1

QD
type: SiteQuality
SIO_000300: 1.131e1

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

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 2591
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 148
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 302
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 218
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 243
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 37136
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2524
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 368
bin: 8.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 879
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 53
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51245
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 735
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3770
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 9.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50073536032656e-5
allele num: 66634
num of homozygotes: 0

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

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

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

FS
type: SiteQuality
SIO_000300: 5.401e0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.928e0

VQSLOD
type: SiteQuality
SIO_000300: -9.16e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 3.9e-1

QD
type: SiteQuality
SIO_000300: 9.119999999999999e0

DP
type: SiteQuality
SIO_000300: 1.567316e6

MQ
type: SiteQuality
SIO_000300: 5.922e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.45e-1

GenotypeDepth
all individuals: 302
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 258
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 337
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 232
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 242
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 158
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3773
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 62
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 51261
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 44
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2522
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 737
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 192
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 873
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 8.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500060002400096e-5
allele num: 66664
num of homozygotes: 0

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

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.634e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.62e-1

QD
type: SiteQuality
SIO_000300: 1.176e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.5e-1

VQSLOD
type: SiteQuality
SIO_000300: 9.3e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.55e-1

FS
type: SiteQuality
SIO_000300: 2.122e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

DP
type: SiteQuality
SIO_000300: 1.568179e6

MQ
type: SiteQuality
SIO_000300: 5.936e1

GenotypeDepth
all individuals: 2604
bin: 3.25e1
variant carriers: 5

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 302
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 254
bin: 6.25e1
variant carriers: 3

GenotypeDepth
all individuals: 243
bin: 5.25e1
variant carriers: 2

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51121
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 80
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3758
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 63
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 101
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 872
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2550
bin: 9.75e1
variant carriers: 29

GenotypeQuality
all individuals: 363
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 732
bin: 7.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66662
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

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

South Asian
type: Population
allele count: 29
allele frequency: 1.756724012599952e-3
allele num: 16508
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: -4.912e0

QD
type: SiteQuality
SIO_000300: 8.18e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 1.49e0

MQ
type: SiteQuality
SIO_000300: 5.1e1

DP
type: SiteQuality
SIO_000300: 1.568426e6

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.09e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.999999999999999e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e-1

GenotypeDepth
all individuals: 254
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 163
bin: 1.25e1
variant carriers: 0

GenotypeDepth
all individuals: 164
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 180
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 220
bin: 6.75e1
variant carriers: 1

GenotypeDepth
all individuals: 305
bin: 9.75e1
variant carriers: 3

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 91
bin: 9.25e1
variant carriers: 5

GenotypeDepth
all individuals: 232
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 55
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 33
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 150
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 8.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 735
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51217
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2546
bin: 9.75e1
variant carriers: 16

GenotypeQuality
all individuals: 35
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 876
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3763
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 9
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 16
allele frequency: 1.855717930874507e-3
allele num: 8622
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9770
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.569279e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.8e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

QD
type: SiteQuality
SIO_000300: 1.403e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.94e0

FS
type: SiteQuality
SIO_000300: 1.79e0

MQRankSum
type: SiteQuality
SIO_000300: 3.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

MQ
type: SiteQuality
SIO_000300: 5.967e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

GenotypeDepth
all individuals: 528
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 29
bin: 2.5e0
variant carriers: 0

GenotypeDepth
all individuals: 180
bin: 7.75e1
variant carriers: 1

GenotypeDepth
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 302
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 251
bin: 6.25e1
variant carriers: 0

GenotypeDepth
all individuals: 246
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 867
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.75e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 84
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 161
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 76
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 741
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3787
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 51099
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 43
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 73
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2520
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66666
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 1
allele frequency: 1.022494887525562e-4
allele num: 9780
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 1.568499e6

FS
type: SiteQuality
SIO_000300: 7.671e0

MQRankSum
type: SiteQuality
SIO_000300: -5.4e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.976e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.06e-1

QD
type: SiteQuality
SIO_000300: 1.199e1

VQSLOD
type: SiteQuality
SIO_000300: 4.08e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.18e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.400000000000001e-2

GenotypeDepth
all individuals: 257
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 243
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 252
bin: 6.25e1
variant carriers: 1

GenotypeDepth
all individuals: 540
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 245
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 60
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 371
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 875
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 163
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 726
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3803
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2519
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 143
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50735
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 191
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 3.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499880009599232e-5
allele num: 66672
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8614
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

VQSLOD
type: SiteQuality
SIO_000300: -2.7e-1

DP
type: SiteQuality
SIO_000300: 1.568911e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.79e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: -1.25e-1

FS
type: SiteQuality
SIO_000300: 4.365e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.104e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e0

QD
type: SiteQuality
SIO_000300: 1.737e1

GenotypeDepth
all individuals: 333
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 231
bin: 7.25e1
variant carriers: 1

GenotypeDepth
all individuals: 257
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2637
bin: 3.25e1
variant carriers: 0

GenotypeDepth
all individuals: 245
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 179
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 245
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 728
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2521
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 189
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 25
bin: 7.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 855
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49995
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 15
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 268
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3758
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 159
bin: 3.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 8.677542519958348e-5
allele num: 11524
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66664
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.05766900896535e-5
allele num: 16508
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8608
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 9.91e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 6.870000000000001e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.0e-3

DP
type: SiteQuality
SIO_000300: 1.567655e6

VQSLOD
type: SiteQuality
SIO_000300: 5.620000000000001e-1

FS
type: SiteQuality
SIO_000300: 7.71e-1

QD
type: SiteQuality
SIO_000300: 1.423e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.28e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeDepth
all individuals: 68
bin: 7.5e0
variant carriers: 0

GenotypeDepth
all individuals: 634
bin: 1.75e1
variant carriers: 0

GenotypeDepth
all individuals: 537
bin: 3.75e1
variant carriers: 0

GenotypeDepth
all individuals: 17632
bin: 2.75e1
variant carriers: 1

GenotypeDepth
all individuals: 335
bin: 4.25e1
variant carriers: 0

GenotypeDepth
all individuals: 156
bin: 8.25e1
variant carriers: 0

GenotypeDepth
all individuals: 86
bin: 9.25e1
variant carriers: 0

GenotypeDepth
all individuals: 245
bin: 5.75e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 143
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 162
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 860
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 50242
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 247
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2521
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 106
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 366
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 247
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3768
bin: 6.75e1
variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9796
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8606
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.000120004800192e-5
allele num: 66664
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.776e0

VQSLOD
type: SiteQuality
SIO_000300: 2.1e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.21e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.87e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.567529e6

QD
type: SiteQuality
SIO_000300: 1.385e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.9e0

GenotypeQuality
all individuals: 446
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24795
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 353
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1057
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 370
bin: 7.25e1
variant carriers: 1

GenotypeQuality
all individuals: 237
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1242
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 371
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1449
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 271
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23583
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 172
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 575
bin: 3.75e1
variant carriers: 1

GenotypeQuality
all individuals: 189
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2825
bin: 9.75e1
variant carriers: 11

South Asian
type: Population
allele count: 13
allele frequency: 1.2531328320802e-3
allele num: 10374
num of homozygotes: 1

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6178
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4162
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5594
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 542
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5490
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 37638
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.754e0

QD
type: SiteQuality
SIO_000300: 1.02e1

DP
type: SiteQuality
SIO_000300: 1.116053e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.78e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.8e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.72e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.7e-3

MQRankSum
type: SiteQuality
SIO_000300: -4.52e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.93e1

GenotypeQuality
all individuals: 790
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1210
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 542
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 455
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 405
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1040
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24403
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 143
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1025
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 169
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1475
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23714
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2815
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 411
bin: 7.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6250
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10442
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5744
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 546
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5592
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4228
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.605252188411838e-5
allele num: 38384
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

MQ
type: SiteQuality
SIO_000300: 5.953e1

DP
type: SiteQuality
SIO_000300: 1.12358e6

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.15e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 4.33e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.67e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.2e-2

QD
type: SiteQuality
SIO_000300: 1.341e1

GenotypeQuality
all individuals: 380
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 407
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 272
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1476
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 540
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1016
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 24388
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 357
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2815
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 231
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 442
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1175
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24160
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 720
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 165
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 430
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6310
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5816
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10482
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 554
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4248
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.579713135899288e-5
allele num: 38764
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 7.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 3.75e-1

QD
type: SiteQuality
SIO_000300: 5.92e0

MQRankSum
type: SiteQuality
SIO_000300: -3.4e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.897e0

VQSLOD
type: SiteQuality
SIO_000300: -9.024e-1

DP
type: SiteQuality
SIO_000300: 1.129841e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.86e-1

GenotypeQuality
all individuals: 527
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1484
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1004
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 409
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 998
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1168
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 491
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24530
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 157
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 756
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 58
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 23992
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2818
bin: 9.75e1
variant carriers: 5

GenotypeQuality
all individuals: 382
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 273
bin: 8.25e1
variant carriers: 1

GenotypeQuality
all individuals: 453
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 5
allele frequency: 1.279164961113385e-4
allele num: 39088
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 558
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5896
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4274
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6326
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 6.94e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.11e1

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.84e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.78e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.133258e6

ClippingRankSum
type: SiteQuality
SIO_000300: -2.3e-1

GenotypeQuality
all individuals: 23592
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 527
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 983
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 403
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2817
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 178
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 480
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 141
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 368
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1485
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 967
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 269
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24816
bin: 6.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 566
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4318
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 7.571551158447327e-5
allele num: 39622
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10572
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5990
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5766
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.096e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.16e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.89e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 7.349e0

DP
type: SiteQuality
SIO_000300: 1.141341e6

VQSLOD
type: SiteQuality
SIO_000300: 3.26e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e-1

QD
type: SiteQuality
SIO_000300: 1.306e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

GenotypeQuality
all individuals: 1514
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 23032
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 424
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1093
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 251
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 544
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 114
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2828
bin: 9.75e1
variant carriers: 13

GenotypeQuality
all individuals: 535
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25075
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 514
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 927
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 910
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1031
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 271
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10682
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5934
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 1.6249593760156e-4
allele num: 6154
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 11
allele frequency: 2.708158944310405e-4
allele num: 40618
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6490
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 574
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4410
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 1.19e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 2.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -1.299e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.799999999999999e-2

DP
type: SiteQuality
SIO_000300: 1.154274e6

FS
type: SiteQuality
SIO_000300: 2.571e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.43e-1

QD
type: SiteQuality
SIO_000300: 1.076e1

GenotypeQuality
all individuals: 404
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 838
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1118
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 300
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2815
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 172
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 262
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 142
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 355
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 987
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1621
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 917
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 23499
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 394
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 524
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 410
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 25186
bin: 6.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6656
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6110
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6526
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4528
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.364289767353887e-5
allele num: 42296
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10966
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 9.05e-1

QD
type: SiteQuality
SIO_000300: 9.869999999999999e0

MQRankSum
type: SiteQuality
SIO_000300: -7.73e-1

FS
type: SiteQuality
SIO_000300: 1.937e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.58e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.2e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.825e0

VQSLOD
type: SiteQuality
SIO_000300: 2.62e-1

DP
type: SiteQuality
SIO_000300: 1.163778e6

GenotypeQuality
all individuals: 256
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1517
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1406
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 4.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 693
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 573
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 752
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 377
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26315
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 740
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 140
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2816
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1521
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 8.25e1
variant carriers: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 586
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4410
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6438
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5888
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.466212883496103e-5
allele num: 40548
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10880
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 1.44e1

MQ
type: SiteQuality
SIO_000300: 5.353e1

MQRankSum
type: SiteQuality
SIO_000300: 9.53e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.7e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.9e-2

BaseQRankSum
type: SiteQuality
SIO_000300: 3.44e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.06e-1

DP
type: SiteQuality
SIO_000300: 1.114449e6

VQSLOD
type: SiteQuality
SIO_000300: -1.037e0

GenotypeQuality
all individuals: 1436
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4743
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2660
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8997
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 1074
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31974
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2818
bin: 9.75e1
variant carriers: 3

GenotypeQuality
all individuals: 348
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2275
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 336
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 3
allele frequency: 2.941176470588235e-4
allele num: 10200
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 34350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4706
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3878
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4724
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 7.23e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

MQ
type: SiteQuality
SIO_000300: 5.958e1

VQSLOD
type: SiteQuality
SIO_000300: 3.06e0

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

DP
type: SiteQuality
SIO_000300: 9.41031e5

QD
type: SiteQuality
SIO_000300: 1.288e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.64e-1

GenotypeDepth
all individuals: 17588
bin: 2.75e1
variant carriers: 0

GenotypeDepth
all individuals: 230
bin: 7.25e1
variant carriers: 0

GenotypeDepth
all individuals: 217
bin: 6.75e1
variant carriers: 0

GenotypeDepth
all individuals: 112
bin: 8.75e1
variant carriers: 0

GenotypeDepth
all individuals: 2618
bin: 3.25e1
variant carriers: 1

GenotypeDepth
all individuals: 256
bin: 4.75e1
variant carriers: 0

GenotypeDepth
all individuals: 242
bin: 5.25e1
variant carriers: 0

GenotypeDepth
all individuals: 302
bin: 9.75e1
variant carriers: 0

GenotypeDepth
all individuals: 307
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 153
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 228
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 182
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 188
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 364
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 171
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2520
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 285
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 276
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3768
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50050
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 858
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 160
bin: 5.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11520
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9792
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.16198001394376e-4
allele num: 8606
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 3.42e-1

DP
type: SiteQuality
SIO_000300: 1.566653e6

QD
type: SiteQuality
SIO_000300: 1.025e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.867e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.98e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.32e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.2e0

GenotypeQuality
all individuals: 336
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2275
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8997
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 922
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1436
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1074
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 156
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 261
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4743
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2660
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 954
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31974
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2818
bin: 9.75e1
variant carriers: 1

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3878
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 2.911208151382824e-5
allele num: 34350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4706
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5598
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10200
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4724
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: -4.06e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.64e-1

QD
type: SiteQuality
SIO_000300: 1.288e1

MQRankSum
type: SiteQuality
SIO_000300: 1.42e-1

FS
type: SiteQuality
SIO_000300: 7.23e-1

DP
type: SiteQuality
SIO_000300: 9.41031e5

VQSLOD
type: SiteQuality
SIO_000300: 3.06e0

MQ
type: SiteQuality
SIO_000300: 5.958e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.07e0

GenotypeQuality
all individuals: 2705
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 239
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5128
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 286
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1049
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 279
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1104
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 939
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2304
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31547
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 330
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2814
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 137
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1729
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 284
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8320
bin: 6.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4636
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 1.802451333813987e-4
allele num: 5548
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10106
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 520
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 33832
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3838
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.782e1

DP
type: SiteQuality
SIO_000300: 9.32127e5

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.000000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: -8.62e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.638e0

QD
type: SiteQuality
SIO_000300: 1.109e1

FS
type: SiteQuality
SIO_000300: 3.287e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.14e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -7.13e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.619e0

GenotypeQuality
all individuals: 6617
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 238
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 456
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 186
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 137
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1109
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 846
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6605
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 325
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 358
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 320
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2815
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 30407
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2389
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 335
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2328
bin: 1.75e1
variant carriers: 0

East Asian
type: Population
allele count: 2
allele frequency: 4.568296025582458e-4
allele num: 4378
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4254
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9882
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 5288
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 32008
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3650
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 502
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 9.04098e5

QD
type: SiteQuality
SIO_000300: 2.43e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.4e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.5e-2

FS
type: SiteQuality
SIO_000300: 5.678e0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.09e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.4e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.67e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.301e0

GenotypeQuality
all individuals: 6462
bin: 7.5e0
variant carriers: 15

GenotypeQuality
all individuals: 309
bin: 9.25e1
variant carriers: 132

GenotypeQuality
all individuals: 1364
bin: 1.75e1
variant carriers: 35

GenotypeQuality
all individuals: 1913
bin: 3.25e1
variant carriers: 28

GenotypeQuality
all individuals: 193
bin: 4.25e1
variant carriers: 27

GenotypeQuality
all individuals: 188
bin: 5.25e1
variant carriers: 48

GenotypeQuality
all individuals: 1131
bin: 1.25e1
variant carriers: 18

GenotypeQuality
all individuals: 773
bin: 3.75e1
variant carriers: 24

GenotypeQuality
all individuals: 714
bin: 2.5e0
variant carriers: 4

GenotypeQuality
all individuals: 5787
bin: 9.75e1
variant carriers: 3234

GenotypeQuality
all individuals: 321
bin: 8.25e1
variant carriers: 101

GenotypeQuality
all individuals: 200
bin: 4.75e1
variant carriers: 51

GenotypeQuality
all individuals: 2454
bin: 2.75e1
variant carriers: 20

GenotypeQuality
all individuals: 139
bin: 5.75e1
variant carriers: 56

GenotypeQuality
all individuals: 266
bin: 7.25e1
variant carriers: 42

GenotypeQuality
all individuals: 266
bin: 8.75e1
variant carriers: 141

GenotypeQuality
all individuals: 30088
bin: 2.25e1
variant carriers: 45

Other
type: Population
allele count: 23
allele frequency: 4.527559055118111e-2
allele num: 508
num of homozygotes: 2

Latino
type: Population
allele count: 104
allele frequency: 2.410755679184052e-2
allele num: 4314
num of homozygotes: 1

East Asian
type: Population
allele count: 309
allele frequency: 6.956325979288609e-2
allele num: 4442
num of homozygotes: 3

South Asian
type: Population
allele count: 894
allele frequency: 8.900836320191159e-2
allele num: 10044
num of homozygotes: 49

European (Finnish)
type: Population
allele count: 108
allele frequency: 2.918918918918919e-2
allele num: 3700
num of homozygotes: 1

African
type: Population
allele count: 43
allele frequency: 8.091832894241625e-3
allele num: 5314
num of homozygotes: 1

European (Non-Finnish)
type: Population
allele count: 1969
allele frequency: 6.053246433841614e-2
allele num: 32528
num of homozygotes: 46

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.7e-3

MQ
type: SiteQuality
SIO_000300: 5.829e1

FS
type: SiteQuality
SIO_000300: 0.0e0

DP
type: SiteQuality
SIO_000300: 9.15421e5

QD
type: SiteQuality
SIO_000300: 1.485e1

VQSLOD
type: SiteQuality
SIO_000300: 3.33e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.26e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.82e0

MQRankSum
type: SiteQuality
SIO_000300: -2.12e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.1e-1

GenotypeQuality
all individuals: 27988
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 349
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2795
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 144
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2499
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 233
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 209
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2294
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10684
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2497
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1103
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4601
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 707
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 1
allele frequency: 2.849002849002849e-4
allele num: 3510
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 27852
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3748
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9224
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 454
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4864
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3352
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.03e0

QD
type: SiteQuality
SIO_000300: 1.458e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.031e0

MQ
type: SiteQuality
SIO_000300: 5.938e1

MQRankSum
type: SiteQuality
SIO_000300: 8.55e-1

DP
type: SiteQuality
SIO_000300: 8.24281e5

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.02e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -7.44e-1

VQSLOD
type: SiteQuality
SIO_000300: -4.183e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
all individuals: 232
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 310
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 555
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 4116
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2570
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 672
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 92
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 26313
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3074
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2756
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 134
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1179
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 5.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3274
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9014
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4718
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 26442
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3250
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 4.036e1

MQRankSum
type: SiteQuality
SIO_000300: -4.21e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.22e-1

QD
type: SiteQuality
SIO_000300: 7.49e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.29e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 7.31e-1

DP
type: SiteQuality
SIO_000300: 8.06909e5

VQSLOD
type: SiteQuality
SIO_000300: -3.231e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.583e0

GenotypeQuality
all individuals: 2602
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 214
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 189
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5313
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6223
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 646
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2195
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1504
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 17505
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2605
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 536
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 241
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2758
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 271
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 133
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 5.75e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 358
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2608
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.194743130227001e-4
allele num: 8370
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 4028
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2792
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 20780
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2096
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.52e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.25e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.167e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.18e0

VQSLOD
type: SiteQuality
SIO_000300: 3.41e-1

DP
type: SiteQuality
SIO_000300: 7.42357e5

BaseQRankSum
type: SiteQuality
SIO_000300: 2.36e0

GenotypeQuality
all individuals: 136
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 718
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2756
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 7339
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2402
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2615
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13813
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 190
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 198
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1541
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10956
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 943
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 459
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1108
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 10453
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 226
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1642
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7970
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2184
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 3600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 5.493298176225006e-5
allele num: 18204
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 342
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2508
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.59e0

MQRankSum
type: SiteQuality
SIO_000300: -4.13e-1

DP
type: SiteQuality
SIO_000300: 7.30273e5

BaseQRankSum
type: SiteQuality
SIO_000300: -1.067e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.26e-2

VQSLOD
type: SiteQuality
SIO_000300: -3.243e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -7.43e-1

MQ
type: SiteQuality
SIO_000300: 3.538e1

QD
type: SiteQuality
SIO_000300: 3.037e1

GenotypeQuality
all individuals: 2965
bin: 9.75e1
variant carriers: 1135

GenotypeQuality
all individuals: 2880
bin: 6.25e1
variant carriers: 37

GenotypeQuality
all individuals: 342
bin: 4.75e1
variant carriers: 36

GenotypeQuality
all individuals: 163
bin: 5.75e1
variant carriers: 64

GenotypeQuality
all individuals: 571
bin: 2.75e1
variant carriers: 64

GenotypeQuality
all individuals: 27389
bin: 7.5e0
variant carriers: 110

GenotypeQuality
all individuals: 1275
bin: 1.75e1
variant carriers: 86

GenotypeQuality
all individuals: 843
bin: 3.25e1
variant carriers: 27

GenotypeQuality
all individuals: 697
bin: 3.75e1
variant carriers: 13

GenotypeQuality
all individuals: 3886
bin: 2.25e1
variant carriers: 97

GenotypeQuality
all individuals: 5019
bin: 2.5e0
variant carriers: 2

GenotypeQuality
all individuals: 213
bin: 8.25e1
variant carriers: 31

GenotypeQuality
all individuals: 245
bin: 7.25e1
variant carriers: 23

GenotypeQuality
all individuals: 193
bin: 9.25e1
variant carriers: 32

GenotypeQuality
all individuals: 310
bin: 7.75e1
variant carriers: 20

GenotypeQuality
all individuals: 157
bin: 8.75e1
variant carriers: 47

GenotypeQuality
all individuals: 637
bin: 6.75e1
variant carriers: 37

African
type: Population
allele count: 81
allele frequency: 3.606411398040962e-2
allele num: 2246
num of homozygotes: 2

East Asian
type: Population
allele count: 2
allele frequency: 3.164556962025316e-3
allele num: 632
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 438
allele frequency: 4.802631578947368e-2
allele num: 9120
num of homozygotes: 14

European (Finnish)
type: Population
allele count: 39
allele frequency: 2.440550688360451e-2
allele num: 1598
num of homozygotes: 1

South Asian
type: Population
allele count: 643
allele frequency: 9.528749259039715e-2
allele num: 6748
num of homozygotes: 30

Latino
type: Population
allele count: 16
allele frequency: 3.80952380952381e-2
allele num: 420
num of homozygotes: 0

Other
type: Population
allele count: 12
allele frequency: 5.309734513274336e-2
allele num: 226
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.52e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -6.6e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

FS
type: SiteQuality
SIO_000300: 5.18e-1

DP
type: SiteQuality
SIO_000300: 4.82091e5

QD
type: SiteQuality
SIO_000300: 1.421e1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.27e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.9e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.87e-1

GenotypeQuality
all individuals: 29885
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 174
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1318
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 545
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1889
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4743
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3432
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 699
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 217
bin: 5.25e1
variant carriers: 1

GenotypeQuality
all individuals: 3619
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 311
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 90
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 652
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2248
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 418
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6794
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9124
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 636
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1604
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 230
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -7.825e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.38e0

QD
type: SiteQuality
SIO_000300: 9.970000000000001e0

MQ
type: SiteQuality
SIO_000300: 5.604e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.38e0

DP
type: SiteQuality
SIO_000300: 4.71956e5

MQRankSum
type: SiteQuality
SIO_000300: -7.2e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.88e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.38e0

GenotypeQuality
all individuals: 1814
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 30946
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 4.25e1
variant carriers: 1

GenotypeQuality
all individuals: 44
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 8220
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 79
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1281
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 731
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1966
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 265
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 326
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6783
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 9.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 678
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.040582726326743e-4
allele num: 9610
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2288
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 1.300390117035111e-4
allele num: 7690
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 8.48e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.7e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.893e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.419999999999999e-2

ClippingRankSum
type: SiteQuality
SIO_000300: 1.96e0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 5.3164e5

GenotypeQuality
all individuals: 6791
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 319
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1163
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6794
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1938
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 852
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 627
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 263
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 108
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1969
bin: 9.75e1
variant carriers: 6

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 674
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 436
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 246
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2264
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1628
num of homozygotes: 0

South Asian
type: Population
allele count: 6
allele frequency: 7.747933884297521e-4
allele num: 7744
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 1.1492e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.013e0

QD
type: SiteQuality
SIO_000300: 8.56e0

DP
type: SiteQuality
SIO_000300: 5.21689e5

VQSLOD
type: SiteQuality
SIO_000300: -5.321e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.68e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.31e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.6e-2

GenotypeQuality
all individuals: 261
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1138
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6787
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 608
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 318
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 44
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6527
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 31439
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 106
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 845
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 70
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1964
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 32
bin: 3.75e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1620
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 434
num of homozygotes: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 1.291989664082687e-4
allele num: 7740
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9516
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2262
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.74e-2

QD
type: SiteQuality
SIO_000300: 1.233e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.65e0

DP
type: SiteQuality
SIO_000300: 5.20022e5

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 5.46e-1

FS
type: SiteQuality
SIO_000300: 2.879e0

ClippingRankSum
type: SiteQuality
SIO_000300: -5.46e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.653e0

VQSLOD
type: SiteQuality
SIO_000300: -1.921e0

GenotypeQuality
all individuals: 836
bin: 6.75e1
variant carriers: 1

GenotypeQuality
all individuals: 314
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 196
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5926
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1984
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 562
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 50
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6739
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 27
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 1.75e1
variant carriers: 1

GenotypeQuality
all individuals: 176
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 120
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1963
bin: 9.75e1
variant carriers: 1

African
type: Population
allele count: 1
allele frequency: 4.397537379067722e-4
allele num: 2274
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 432
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9484
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 670
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7722
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1604
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -6.859999999999999e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.984e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e-1

DP
type: SiteQuality
SIO_000300: 5.13757e5

QD
type: SiteQuality
SIO_000300: 1.209e1

FS
type: SiteQuality
SIO_000300: 1.32e0

MQRankSum
type: SiteQuality
SIO_000300: 7.42e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.58e-1

GenotypeQuality
all individuals: 54
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1936
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 6503
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32147
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 194
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 637
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 137
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 68
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4847
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1961
bin: 9.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 41
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 476
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 121
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2254
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 1598
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 428
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 648
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9392
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 244
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.98e-1

DP
type: SiteQuality
SIO_000300: 5.01259e5

QD
type: SiteQuality
SIO_000300: 1.226e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -7.12e-2

MQRankSum
type: SiteQuality
SIO_000300: 4.06e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 2.454e0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.06e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -7.28e-1

GenotypeQuality
all individuals: 65
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30912
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 147
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 449
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3533
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 42
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 328
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5497
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2402
bin: 2.5e0
variant carriers: 0