18-31523153-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31523153
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31523154
    reference: chr 18
allele count: 7
allele frequency: 6.121235440204274e-5
allele num: 114356
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*846-12_*846-11insC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+15049_1236+15050insC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1189-12_1189-11insC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.484-12_484-11insC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1429-12_1429-11insC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.574-12_574-11insC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1207-12_1207-11insC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.772-12_772-11insC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+15049_894+15050insC
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4047
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23198
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16435
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 976
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2049
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 411
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6140
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1314
  bin: 9.75e1
  variant carriers: 7
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: DP

18-31523153-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31523153
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31523153
    reference: chr 18
allele count: 1
allele frequency: 8.744622057434678e-6
allele num: 114356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+15050T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.772-11T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1429-11T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.484-11T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.574-11T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1189-11T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1207-11T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+15050T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*846-11T>C
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1304
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4829
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 488
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23198
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4047
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4731
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2531
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1254
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16435
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 865
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 402
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 227
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 980
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ

18-31523154-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31523154
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31523154
    reference: chr 18
allele count: 7
allele frequency: 6.145418151809386e-5
allele num: 113906
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1429-12T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.772-12T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+15049T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.484-12T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1207-12T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1189-12T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+15049T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*846-12T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.574-12T>C
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1303
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 483
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 265
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1260
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4044
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4806
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2555
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16383
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23173
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8007
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 132
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 836
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 934
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 907
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: East Asian
reference allele: A
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

18-31523155-A-AG
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31523155
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31523156
    reference: chr 18
allele count: 5
allele frequency: 4.436793440644577e-5
allele num: 112694
alternate allele: AG
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.772-14dupC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*846-14dupC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1189-14dupC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1429-14dupC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1207-14dupC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.574-14dupC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+15047dupC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+15047dupC
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.484-14dupC
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: VQSRTrancheINDEL97.00to99.00
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22363
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3948
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 871
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4614
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 124
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1238
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 260
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15753
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 470
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1609
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1189
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7607
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1008
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: Other
reference allele: A
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ

18-31523158-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31523158
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31523158
    reference: chr 18
allele count: 1
allele frequency: 9.05173974437887e-6
allele num: 110476
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+15045C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1207-16C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1189-16C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.484-16C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.574-16C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+15045C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*846-16C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.772-16C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1429-16C>A
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4521
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1110
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20483
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2402
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10199
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3880
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2854
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 188
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 329
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 57
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13157
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1105
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 281
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 272
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 794
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1076
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1142
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: MQ

18-31523162-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31523162
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31523162
    reference: chr 18
allele count: 1
allele frequency: 9.068156262468716e-6
allele num: 110276
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.772-20T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+15041T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1429-20T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*846-20T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.484-20T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1189-20T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1207-20T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+15041T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.574-20T>A
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20799
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 39
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2404
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10854
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4076
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1197
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12189
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2392
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 280
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1119
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 527
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1266
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 241
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 243
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-31523167-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31523167
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31523166
    reference: chr 18
allele count: 8
allele frequency: 7.380482314519254e-5
allele num: 108394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.574-26delT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.772-26delT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1189-26delT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1429-26delT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*846-26delT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+15035delT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1207-26delT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+15035delT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.484-26delT
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2042
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10085
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 36
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 1.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14232
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18265
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1379
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4760
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 266
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 314
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 446
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 271
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 997
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13755
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: African
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: GA
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: QD

18-31523175-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31523175
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31523175
    reference: chr 18
allele count: 1
allele frequency: 9.501548752446648e-6
allele num: 105246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*846-33A>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1429-33A>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+15028A>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1189-33A>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1207-33A>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.772-33A>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.574-33A>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+15028A>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.484-33A>T
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5394
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 256
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1975
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 511
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5671
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9949
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11105
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1403
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19701
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 169
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3719
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 558
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7050
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15905
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 570
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 616
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: MQ
site quality: ReadPosRankSum
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD

18-31523184-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31523184
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31523184
    reference: chr 18
allele count: 1
allele frequency: 9.9657179303197e-6
allele num: 100344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.574-42C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+15019C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1189-42C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+15019C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.484-42C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1207-42C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*846-42C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1429-42C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.772-42C>T
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18847
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15267
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1415
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6369
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 465
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1876
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2433
  bin: 4.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: G
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD

18-31523184-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31523184
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31523184
    reference: chr 18
allele count: 1
allele frequency: 9.9657179303197e-6
allele num: 100344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.484-42C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1207-42C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+15019C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1189-42C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.574-42C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*846-42C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+15019C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1429-42C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.772-42C>A
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7352
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4636
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18847
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1022
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6452
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15267
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2287
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1389
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2433
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2572
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 562
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 821
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD

18-31537246-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537246
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537246
    reference: chr 18
allele count: 1
allele frequency: 8.809175637343858e-6
allele num: 113518
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+957C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+957C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+957C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.573+44C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1206+44C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+957C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+957C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+957C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1428+44C>T
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8376
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 750
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 674
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 440
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1038
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1482
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2121
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13420
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27833
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 850
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 663
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 555
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 489
  bin: 4.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD

18-31537262-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537262
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537263
    reference: chr 18
allele count: 1
allele frequency: 8.767930417704205e-6
allele num: 114052
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+940dupT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+940dupT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+940dupT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+940dupT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1206+27dupT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+940dupT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+940dupT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.573+27dupT
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1428+27dupT
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28190
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14341
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1853
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 328
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 478
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 340
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 666
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1467
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8371
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 115
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2343
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2873
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: T
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: ReadPosRankSum

18-31537265-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537265
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537265
    reference: chr 18
allele count: 1
allele frequency: 8.75702751458045e-6
allele num: 114194
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+938C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+938C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+938C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+938C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.573+25C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1206+25C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+938C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1428+25C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+938C>T
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 373
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2341
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 96
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD

18-31537265-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537265
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537265
    reference: chr 18
allele count: 5
allele frequency: 4.378513757290226e-5
allele num: 114194
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+938C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+938C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1428+25C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+938C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+938C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.573+25C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1206+25C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+938C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+938C>A
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 392
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14505
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 669
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1466
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 88
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8370
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1777
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 151
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2947
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 971
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 73
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 169
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: South Asian
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD
site quality: DP

18-31537270-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537270
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537270
    reference: chr 18
allele count: 3
allele frequency: 2.616978959489166e-5
allele num: 114636
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1428+20A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+933A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+933A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+933A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1206+20A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.573+20A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+933A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+933A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+933A>G
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8378
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 327
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3001
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 283
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1672
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14773
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 28295
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 75
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38658
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 653
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2335
  bin: 9.75e1
  variant carriers: 3
genotype quality: GenotypeQuality
  all individuals: 283
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum

18-31537320-GCAGGACTTGAGGT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537320
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537307
    reference: chr 18
allele count: 1
allele frequency: 8.296138976920141e-6
allele num: 120538
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsp: ENSP00000443472.1:p.Tyr388SerfsTer4
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsp: ENSP00000261592.4:p.Tyr462SerfsTer4
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsp: ENSP00000445733.1:p.Tyr177SerfsTer4
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 18175
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 401
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29348
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8468
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 213
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8706
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2099
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 361
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Tyr462SerfsTer4
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
reference allele: GCAGGACTTGAGGT
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: MQ

18-31537325-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537325
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537325
    reference: chr 18
allele count: 1
allele frequency: 8.278008642241022e-6
allele num: 120802
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+878T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+878T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1171T>A
  hgvsp: ENSP00000443472.1:p.Ser391Thr
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+878T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1393T>A
  hgvsp: ENSP00000261592.4:p.Ser465Thr
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+878T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+878T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+878T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.538T>A
  hgvsp: ENSP00000445733.1:p.Ser180Thr
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29451
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 270
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18298
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8471
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43092
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser465Thr
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: QD

18-31537329-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537329
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537329
    reference: chr 18
allele count: 1
allele frequency: 8.269656974628692e-6
allele num: 120924
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+874C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.534C>T
  hgvsp: ENST00000535384.1:c.534C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+874C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+874C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1389C>T
  hgvsp: ENST00000261592.5:c.1389C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1167C>T
  hgvsp: ENST00000538587.1:c.1167C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+874C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+874C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+874C>T
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8480
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29505
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18343
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 107
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 53
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 414
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu463Leu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum

18-31537339-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537339
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537339
    reference: chr 18
allele count: 3
allele frequency: 2.478150968957029e-5
allele num: 121058
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+864G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+864G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1379G>A
  hgvsp: ENSP00000261592.4:p.Arg460His
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+864G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.524G>A
  hgvsp: ENSP00000445733.1:p.Arg175His
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1157G>A
  hgvsp: ENSP00000443472.1:p.Arg386His
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+864G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+864G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+864G>A
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 29573
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18358
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 144
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 171
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg460His
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
population: East Asian
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum

18-31537340-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537340
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537340
    reference: chr 18
allele count: 1
allele frequency: 8.260230295220631e-6
allele num: 121062
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+863C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+863C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.523C>A
  hgvsp: ENSP00000445733.1:p.Arg175Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1156C>A
  hgvsp: ENSP00000443472.1:p.Arg386Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+863C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+863C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1378C>A
  hgvsp: ENSP00000261592.4:p.Arg460Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+863C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+863C>A
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18367
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29578
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1465
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8503
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 358
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2098
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Arg460Ser
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD

18-31537344-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537344
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537344
    reference: chr 18
allele count: 1
allele frequency: 8.256683785524381e-6
allele num: 121114
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+859T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+859T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1152T>A
  hgvsp: ENST00000538587.1:c.1152T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.519T>A
  hgvsp: ENST00000535384.1:c.519T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+859T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+859T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1374T>A
  hgvsp: ENST00000261592.5:c.1374T>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+859T>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+859T>A
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 122
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29595
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8500
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1463
  bin: 3.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 145
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 975
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43379
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Arg458Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: European (Finnish)
population: Other
population: East Asian
population: South Asian
reference allele: A
site quality: DP
site quality: MQ
site quality: FS
site quality: QD
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum

18-31537346-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537346
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537346
    reference: chr 18
allele count: 1
allele frequency: 8.256820133430213e-6
allele num: 121112
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+857C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+857C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1150C>A
  hgvsp: ENSP00000443472.1:p.Arg384Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1372C>A
  hgvsp: ENSP00000261592.4:p.Arg458Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.517C>A
  hgvsp: ENSP00000445733.1:p.Arg173Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+857C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+857C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+857C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+857C>A
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18373
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 120
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8505
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29603
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 974
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 416
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg458Ser
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: ClippingRankSum

18-31537347-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537347
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537347
    reference: chr 18
allele count: 1
allele frequency: 8.256547442121603e-6
allele num: 121116
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+856A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+856A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1371A>G
  hgvsp: ENST00000261592.5:c.1371A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.516A>G
  hgvsp: ENST00000535384.1:c.516A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+856A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+856A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1149A>G
  hgvsp: ENST00000538587.1:c.1149A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+856A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+856A>G
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: synonymous
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 119
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29606
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1464
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 436
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18376
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8504
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 141
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Lys457Lys
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: DP
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum

18-31537382-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537382
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537382
    reference: chr 18
allele count: 3
allele frequency: 2.477373323644051e-5
allele num: 121096
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.481C>A
  hgvsp: ENST00000535384.1:c.481C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+821C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+821C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1114C>A
  hgvsp: ENST00000538587.1:c.1114C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+821C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+821C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+821C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1336C>A
  hgvsp: ENST00000261592.5:c.1336C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+821C>A
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 664
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8521
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 437
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18292
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 133
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29630
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Arg446Arg
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/18-31537430-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537430
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537430
    reference: chr 18
allele count: 1
allele frequency: 8.294212298657997e-6
allele num: 120566
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+773T>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+773T>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1288T>G
  hgvsp: ENSP00000261592.4:p.Ser430Ala
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1066T>G
  hgvsp: ENSP00000443472.1:p.Ser356Ala
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+773T>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+773T>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+773T>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.433T>G
  hgvsp: ENSP00000445733.1:p.Ser145Ala
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+773T>G
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8467
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 355
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 661
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17881
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 435
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1453
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 325
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29475
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2071
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 412
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser430Ala
num of homozygotes: 0
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum

18-31537444-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537444
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537444
    reference: chr 18
allele count: 1
allele frequency: 8.3380582329987e-6
allele num: 119932
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1274G>A
  hgvsp: ENSP00000261592.4:p.Arg425Gln
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+759G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+759G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+759G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1052G>A
  hgvsp: ENSP00000443472.1:p.Arg351Gln
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.419G>A
  hgvsp: ENSP00000445733.1:p.Arg140Gln
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+759G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+759G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+759G>A
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29105
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1440
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8334
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 668
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17446
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8328
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41890
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 173
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg425Gln
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: QD

18-31537452-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537452
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537452
    reference: chr 18
allele count: 30
allele frequency: 2.514668901927913e-4
allele num: 119300
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+751C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+751C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+751C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1044C>T
  hgvsp: ENST00000538587.1:c.1044C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1266C>T
  hgvsp: ENST00000261592.5:c.1266C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+751C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.411C>T
  hgvsp: ENST00000535384.1:c.411C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+751C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+751C>T
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1340
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28739
  bin: 2.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 430
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 1405
  bin: 3.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17128
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 486
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 644
  bin: 4.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 931
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 326
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 5.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 8071
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 55
  bin: 9.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 327
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 400
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 335
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Asn422Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
population: East Asian
population: South Asian
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff

18-31537469-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537469
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537469
    reference: chr 18
allele count: 1
allele frequency: 8.540730744922536e-6
allele num: 117086
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1027C>A
  hgvsp: ENSP00000443472.1:p.Leu343Met
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+734C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+734C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+734C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+734C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.394C>A
  hgvsp: ENSP00000445733.1:p.Leu132Met
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+734C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+734C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1249C>A
  hgvsp: ENSP00000261592.4:p.Leu417Met
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 16021
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 217
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 631
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1980
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26619
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1208
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3450
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7462
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 894
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 813
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37939
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 383
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Leu417Met
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: FS

18-31537487-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537487
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537487
    reference: chr 18
allele count: 1
allele frequency: 8.842514811212309e-6
allele num: 113090
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+716C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+716C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.382-6C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+716C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1237-6C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1015-6C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+716C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+716C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+716C>G
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 611
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 418
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6356
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1217
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2342
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22827
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8640
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12815
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1417
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1406
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 265
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8727
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 3.25e1
  variant carriers: 0
hgvs: c.1237-6C>G
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: East Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD

18-31537505-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537505
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537505
    reference: chr 18
allele count: 2
allele frequency: 1.84372580109886e-5
allele num: 108476
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1237-24C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+698C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+698C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+698C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.382-24C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+698C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+698C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1015-24C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+698C>T
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 507
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3788
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 966
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6362
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17607
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14294
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9090
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5641
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4525
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 257
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 109
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20234
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3098
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 524
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: QD

18-31537517-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537517
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537517
    reference: chr 18
allele count: 1
allele frequency: 9.537434430138293e-6
allele num: 104850
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+686C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1015-36C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+686C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+686C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+686C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.382-36C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1237-36C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+686C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+686C>G
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7640
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19888
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13611
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 984
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6083
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6778
  bin: 7.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 867
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2394
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14818
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 493
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1706
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1306
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 744
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5707
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

18-31537524-GCT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31537524
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31537522
    reference: chr 18
allele count: 1
allele frequency: 9.914340101522842e-6
allele num: 100864
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+677_1236+678delAG
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+677_483+678delAG
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+677_*845+678delAG
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.382-45_382-44delAG
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+677_894+678delAG
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+677_1188+678delAG
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1015-45_1015-44delAG
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+677_771+678delAG
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1237-45_1237-44delAG
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: VQSRTrancheINDEL99.50to99.90
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 562
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 826
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16015
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6621
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8241
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19168
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4455
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 131
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 215
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 654
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7213
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1784
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 229
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2236
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
reference allele: GCT
site quality: MQ
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum

18-31538155-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538155
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538155
    reference: chr 18
allele count: 2
allele frequency: 1.693766937669377e-5
allele num: 118080
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+48T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+48T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1014+48T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+48T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+48T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.381+48T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+48T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1236+48T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+48T>C
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6013
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2222
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2570
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1462
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9020
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6389
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 587
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1152
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9806
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1704
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1192
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 944
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 697
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9652
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22610
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 467
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff

18-31538158-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538158
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538158
    reference: chr 18
allele count: 215
allele frequency: 1.822466347946971e-3
allele num: 117972
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+45C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+45C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+45C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+45C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.381+45C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+45C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1014+45C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+45C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1236+45C>T
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2560
  bin: 1.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 2446
  bin: 2.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 7872
  bin: 4.25e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 1712
  bin: 6.25e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 7.5e0
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4152
  bin: 5.25e1
  variant carriers: 23
genotype depth: GenotypeDepth
  all individuals: 585
  bin: 7.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 1.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 2725
  bin: 5.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 9827
  bin: 3.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 6011
  bin: 4.75e1
  variant carriers: 24
genotype depth: GenotypeDepth
  all individuals: 825
  bin: 7.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 9016
  bin: 3.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1194
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 1161
  bin: 6.75e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 471
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6449
  bin: 2.75e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 437
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 900
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 691
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5526
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 276
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 62
  bin: 5.75e1
  variant carriers: 1
num of homozygotes: 1
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: BaseQRankSum

18-31538161-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538161
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538161
    reference: chr 18
allele count: 1
allele frequency: 8.4742890071523e-6
allele num: 118004
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+42C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+42C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1236+42C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.381+42C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+42C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+42C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1014+42C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+42C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+42C>T
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6511
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9024
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2514
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 824
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9877
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2712
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2700
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6005
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5564
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1417
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 189
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
reference allele: G
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff

18-31538163-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538163
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538163
    reference: chr 18
allele count: 1
allele frequency: 8.456373568758774e-6
allele num: 118254
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+40C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.381+40C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+40C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+40C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+40C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+40C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1236+40C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1014+40C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+40C>T
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 116
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1398
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2713
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2465
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1188
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2837
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6542
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1148
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 469
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4139
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1700
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1088
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9027
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 581
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9913
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1002
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2310
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4219
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2148
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: Latino
population: European (Finnish)
population: East Asian
population: South Asian
population: African
reference allele: G
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum

18-31538181-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538181
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538181
    reference: chr 18
allele count: 70
allele frequency: 5.884726612415092e-4
allele num: 118952
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+22G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+22G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+22G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+22G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.381+22G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+22G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1236+22G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+22G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1014+22G>A
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6877
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9021
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 9.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 6.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 6.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 7870
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9958
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5998
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 1.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 9.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 5.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.75e1
  variant carriers: 8
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 454
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 5682
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: South Asian
population: Latino
population: Other
population: European (Finnish)
population: African
population: European (Non-Finnish)
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: MQRankSum

18-31538181-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538181
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538180
    reference: chr 18
allele count: 1
allele frequency: 8.406752303450132e-6
allele num: 118952
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1014+21delA
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.381+21delA
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+21delA
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+21delA
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+21delA
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1236+21delA
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+21delA
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+21delA
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+21delA
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 586
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1349
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4664
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5998
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 823
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9021
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1105
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7870
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6877
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2704
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1211
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1703
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9958
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1145
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1210
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 332
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5682
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22508
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Other
population: Latino
population: European (Finnish)
reference allele: CT
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: DP

18-31538182-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538182
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538182
    reference: chr 18
allele count: 1
allele frequency: 8.39560070523046e-6
allele num: 119110
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.381+21A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+21A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+21A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+21A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+21A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+21A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1014+21A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+21A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1236+21A>G
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9029
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1285
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4771
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1069
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 344
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6004
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6906
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2708
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9966
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22463
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 315
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2324
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ

18-31538187-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538187
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538187
    reference: chr 18
allele count: 2
allele frequency: 1.674116485025028e-5
allele num: 119466
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+16C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+16C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1014+16C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+16C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+16C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1236+16C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+16C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+16C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.381+16C>T
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9987
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9028
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6991
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 908
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 926
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5253
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 281
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 996
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13381
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4112
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 74
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: European (Finnish)
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

http://identifiers.org/exac.variant/18-31538193-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538193
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538193
    reference: chr 18
allele count: 1
allele frequency: 8.344737808338063e-6
allele num: 119836
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+10G>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+10G>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+10G>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1014+10G>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+10G>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+10G>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1236+10G>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.381+10G>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+10G>T
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7192
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5480
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 687
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 249
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 699
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10035
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 201
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4118
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 240
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22465
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2338
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD

18-31538196-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538196
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538196
    reference: chr 18
allele count: 1
allele frequency: 8.322237017310253e-6
allele num: 120160
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+7C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+7C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+7C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1014+7C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1236+7C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.381+7C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+7C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+7C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+7C>G
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 218
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7276
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5687
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6004
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4132
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1142
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2709
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10033
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2151
  bin: 8.75e1
  variant carriers: 0
hgvs: c.1236+7C>G
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Other
population: African
population: East Asian
reference allele: G
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: DP

18-31538197-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538197
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538197
    reference: chr 18
allele count: 1
allele frequency: 8.318221896887321e-6
allele num: 120218
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+6T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1014+6T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1236+6T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.381+6T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+6T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+6T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+6T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+6T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+6T>C
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.80to99.90
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2711
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7872
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 534
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1187
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9033
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 535
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1701
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10034
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6008
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5730
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14058
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
hgvs: c.1236+6T>C
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: African
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
reference allele: A
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQRankSum

18-31538200-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538200
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538200
    reference: chr 18
allele count: 1
allele frequency: 8.307027745472669e-6
allele num: 120380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.483+3G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.1014+3G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.381+3G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1188+3G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1236+3G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1236+3G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.894+3G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*845+3G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.771+3G>A
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 432
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5792
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9035
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7874
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 455
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6009
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7432
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1186
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 466
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10055
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1698
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
hgvs: c.1236+3G>A
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: African
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum

18-31538220-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538220
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538220
    reference: chr 18
allele count: 1
allele frequency: 8.261458643138033e-6
allele num: 121044
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.877C>T
  hgvsp: ENSP00000269185.4:p.Arg293Trp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.754C>T
  hgvsp: ENSP00000438190.1:p.Arg252Trp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.466C>T
  hgvsp: ENSP00000467015.1:p.Arg156Trp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.997C>T
  hgvsp: ENSP00000443472.1:p.Arg333Trp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1171C>T
  hgvsp: ENSP00000467629.1:p.Arg391Trp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.364C>T
  hgvsp: ENSP00000445733.1:p.Arg122Trp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1219C>T
  hgvsp: ENSP00000465450.1:p.Arg407Trp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1219C>T
  hgvsp: ENSP00000261592.4:p.Arg407Trp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*828C>T
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10153
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6007
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2154
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5926
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg407Trp
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

18-31538220-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538220
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538220
    reference: chr 18
allele count: 12
allele frequency: 9.91375037176564e-5
allele num: 121044
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.997C>A
  hgvsp: ENST00000538587.1:c.997C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.364C>A
  hgvsp: ENST00000535384.1:c.364C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*828C>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.754C>A
  hgvsp: ENST00000535475.1:c.754C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1219C>A
  hgvsp: ENST00000589544.1:c.1219C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.877C>A
  hgvsp: ENST00000269185.4:c.877C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1171C>A
  hgvsp: ENST00000590712.1:c.1171C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1219C>A
  hgvsp: ENST00000261592.5:c.1219C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.466C>A
  hgvsp: ENST00000586553.1:c.466C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1140
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 467
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7861
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1699
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6022
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4131
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 579
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6007
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2707
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1190
  bin: 9.75e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9037
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10153
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Arg407Arg
num of homozygotes: 0
population: Other
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum
site quality: DP

18-31538224-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538224
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538224
    reference: chr 18
allele count: 295
allele frequency: 2.435198943371306e-3
allele num: 121140
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.750C>T
  hgvsp: ENST00000535475.1:c.750C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.993C>T
  hgvsp: ENST00000538587.1:c.993C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.360C>T
  hgvsp: ENST00000535384.1:c.360C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.462C>T
  hgvsp: ENST00000586553.1:c.462C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1167C>T
  hgvsp: ENST00000590712.1:c.1167C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1215C>T
  hgvsp: ENST00000261592.5:c.1215C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1215C>T
  hgvsp: ENST00000589544.1:c.1215C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.873C>T
  hgvsp: ENST00000269185.4:c.873C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*824C>T
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7861
  bin: 4.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5984
  bin: 4.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 7925
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 816
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1408
  bin: 9.75e1
  variant carriers: 244
genotype depth: GenotypeDepth
  all individuals: 463
  bin: 8.25e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 5.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10149
  bin: 3.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6023
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 110
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 360
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9019
  bin: 3.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 6.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15182
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ala405Ala
num of homozygotes: 2
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
population: European (Finnish)
population: South Asian
reference allele: G
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS

18-31538225-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538225
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538225
    reference: chr 18
allele count: 1
allele frequency: 8.254366559910193e-6
allele num: 121148
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.872C>T
  hgvsp: ENSP00000269185.4:p.Ala291Val
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.749C>T
  hgvsp: ENSP00000438190.1:p.Ala250Val
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.992C>T
  hgvsp: ENSP00000443472.1:p.Ala331Val
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1214C>T
  hgvsp: ENSP00000465450.1:p.Ala405Val
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.461C>T
  hgvsp: ENSP00000467015.1:p.Ala154Val
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1214C>T
  hgvsp: ENSP00000261592.4:p.Ala405Val
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1166C>T
  hgvsp: ENSP00000467629.1:p.Ala389Val
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*823C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.359C>T
  hgvsp: ENSP00000445733.1:p.Ala120Val
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6015
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9057
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7901
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4128
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10202
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7962
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2362
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15262
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ala405Val
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: Latino
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

18-31538226-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538226
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538226
    reference: chr 18
allele count: 1
allele frequency: 8.253412786187088e-6
allele num: 121162
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1165G>A
  hgvsp: ENSP00000467629.1:p.Ala389Thr
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.871G>A
  hgvsp: ENSP00000269185.4:p.Ala291Thr
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*822G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1213G>A
  hgvsp: ENSP00000465450.1:p.Ala405Thr
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1213G>A
  hgvsp: ENSP00000261592.4:p.Ala405Thr
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.748G>A
  hgvsp: ENSP00000438190.1:p.Ala250Thr
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.358G>A
  hgvsp: ENSP00000445733.1:p.Ala120Thr
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.991G>A
  hgvsp: ENSP00000443472.1:p.Ala331Thr
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.460G>A
  hgvsp: ENSP00000467015.1:p.Ala154Thr
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10209
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1173
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 820
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9059
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6033
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 58
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7899
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6017
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5963
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4163
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Ala405Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff

18-31538232-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538232
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538232
    reference: chr 18
allele count: 3
allele frequency: 2.475165836111019e-5
allele num: 121204
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.352G>A
  hgvsp: ENSP00000445733.1:p.Val118Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.742G>A
  hgvsp: ENSP00000438190.1:p.Val248Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1159G>A
  hgvsp: ENSP00000467629.1:p.Val387Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.985G>A
  hgvsp: ENSP00000443472.1:p.Val329Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*816G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.865G>A
  hgvsp: ENSP00000269185.4:p.Val289Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.454G>A
  hgvsp: ENSP00000467015.1:p.Val152Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1207G>A
  hgvsp: ENSP00000465450.1:p.Val403Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1207G>A
  hgvsp: ENSP00000261592.4:p.Val403Ile
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6038
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 41
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9063
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4129
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 361
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 461
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8005
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10207
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1666
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6016
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1128
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7904
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1174
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Val403Ile
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum

18-31538235-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538235
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538235
    reference: chr 18
allele count: 140
allele frequency: 1.154791560123398e-3
allele num: 121234
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.451G>A
  hgvsp: ENSP00000467015.1:p.Gly151Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1204G>A
  hgvsp: ENSP00000261592.4:p.Gly402Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1156G>A
  hgvsp: ENSP00000467629.1:p.Gly386Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.739G>A
  hgvsp: ENSP00000438190.1:p.Gly247Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.862G>A
  hgvsp: ENSP00000269185.4:p.Gly288Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*813G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1204G>A
  hgvsp: ENSP00000465450.1:p.Gly402Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.982G>A
  hgvsp: ENSP00000443472.1:p.Gly328Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.349G>A
  hgvsp: ENSP00000445733.1:p.Gly117Ser
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7895
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 462
  bin: 8.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6029
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1270
  bin: 9.75e1
  variant carriers: 109
genotype depth: GenotypeDepth
  all individuals: 821
  bin: 7.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 5.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 9045
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8029
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10191
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1127
  bin: 6.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6001
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 4116
  bin: 5.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1661
  bin: 6.25e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5965
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4255
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22376
  bin: 9.75e1
  variant carriers: 139
genotype quality: GenotypeQuality
  all individuals: 2160
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Gly402Ser
num of homozygotes: 1
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Latino
population: Other
population: African
population: East Asian
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: ClippingRankSum

18-31538236-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538236
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538236
    reference: chr 18
allele count: 6
allele frequency: 4.948616861587186e-5
allele num: 121246
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.450C>T
  hgvsp: ENST00000586553.1:c.450C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*812C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1203C>T
  hgvsp: ENST00000261592.5:c.1203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.738C>T
  hgvsp: ENST00000535475.1:c.738C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.861C>T
  hgvsp: ENST00000269185.4:c.861C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1203C>T
  hgvsp: ENST00000589544.1:c.1203C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.981C>T
  hgvsp: ENST00000538587.1:c.981C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.348C>T
  hgvsp: ENST00000535384.1:c.348C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1155C>T
  hgvsp: ENST00000590712.1:c.1155C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6037
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 31
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 9073
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10215
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 8055
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4264
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp401Asp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: African
population: Latino
population: Other
reference allele: G
site quality: MQ
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

18-31538240-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538240
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538240
    reference: chr 18
allele count: 3
allele frequency: 2.473573984597879e-5
allele num: 121282
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*808C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.446C>T
  hgvsp: ENSP00000467015.1:p.Thr149Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.734C>T
  hgvsp: ENSP00000438190.1:p.Thr245Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.977C>T
  hgvsp: ENSP00000443472.1:p.Thr326Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.857C>T
  hgvsp: ENSP00000269185.4:p.Thr286Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1151C>T
  hgvsp: ENSP00000467629.1:p.Thr384Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1199C>T
  hgvsp: ENSP00000465450.1:p.Thr400Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.344C>T
  hgvsp: ENSP00000445733.1:p.Thr115Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1199C>T
  hgvsp: ENSP00000261592.4:p.Thr400Ile
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7905
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4171
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4264
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Thr400Ile
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
population: African
population: East Asian
population: South Asian
reference allele: G
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: MQ

18-31538240-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538240
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538240
    reference: chr 18
allele count: 1
allele frequency: 8.245246615326264e-6
allele num: 121282
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1151C>G
  hgvsp: ENSP00000467629.1:p.Thr384Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.344C>G
  hgvsp: ENSP00000445733.1:p.Thr115Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.446C>G
  hgvsp: ENSP00000467015.1:p.Thr149Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*808C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.857C>G
  hgvsp: ENSP00000269185.4:p.Thr286Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1199C>G
  hgvsp: ENSP00000261592.4:p.Thr400Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1199C>G
  hgvsp: ENSP00000465450.1:p.Thr400Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.734C>G
  hgvsp: ENSP00000438190.1:p.Thr245Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.977C>G
  hgvsp: ENSP00000443472.1:p.Thr326Arg
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8059
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6051
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2680
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4122
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 54
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 10217
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7905
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3933
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2370
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Thr400Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: G
site quality: FS
site quality: DP
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum

18-31538246-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538246
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538246
    reference: chr 18
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.440A>T
  hgvsp: ENSP00000467015.1:p.Asn147Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1193A>T
  hgvsp: ENSP00000465450.1:p.Asn398Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.851A>T
  hgvsp: ENSP00000269185.4:p.Asn284Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1145A>T
  hgvsp: ENSP00000467629.1:p.Asn382Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.338A>T
  hgvsp: ENSP00000445733.1:p.Asn113Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.971A>T
  hgvsp: ENSP00000443472.1:p.Asn324Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1193A>T
  hgvsp: ENSP00000261592.4:p.Asn398Ile
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*802A>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.728A>T
  hgvsp: ENSP00000438190.1:p.Asn243Ile
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4171
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2170
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asn398Ile
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: MQ
site quality: FS

18-31538246-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538246
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538246
    reference: chr 18
allele count: 1
allele frequency: 8.24279991427488e-6
allele num: 121318
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1193A>G
  hgvsp: ENSP00000261592.4:p.Asn398Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.440A>G
  hgvsp: ENSP00000467015.1:p.Asn147Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*802A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.728A>G
  hgvsp: ENSP00000438190.1:p.Asn243Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1145A>G
  hgvsp: ENSP00000467629.1:p.Asn382Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.971A>G
  hgvsp: ENSP00000443472.1:p.Asn324Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.851A>G
  hgvsp: ENSP00000269185.4:p.Asn284Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1193A>G
  hgvsp: ENSP00000465450.1:p.Asn398Ser
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.338A>G
  hgvsp: ENSP00000445733.1:p.Asn113Ser
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8068
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10218
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9072
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 42
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6061
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2170
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15441
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asn398Ser
num of homozygotes: 0
population: Other
population: European (Finnish)
population: African
population: South Asian
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ

18-31538254-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538254
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538254
    reference: chr 18
allele count: 1
allele frequency: 8.241577108195424e-6
allele num: 121336
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1185G>C
  hgvsp: ENSP00000465450.1:p.Glu395Asp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1137G>C
  hgvsp: ENSP00000467629.1:p.Glu379Asp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1185G>C
  hgvsp: ENSP00000261592.4:p.Glu395Asp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.432G>C
  hgvsp: ENSP00000467015.1:p.Glu144Asp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.330G>C
  hgvsp: ENSP00000445733.1:p.Glu110Asp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*794G>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.963G>C
  hgvsp: ENSP00000443472.1:p.Glu321Asp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.843G>C
  hgvsp: ENSP00000269185.4:p.Glu281Asp
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.720G>C
  hgvsp: ENSP00000438190.1:p.Glu240Asp
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1167
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 30
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10220
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1659
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 459
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8073
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 819
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5987
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Glu395Asp
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: South Asian
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD

18-31538257-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538257
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538257
    reference: chr 18
allele count: 1
allele frequency: 8.241033755274261e-6
allele num: 121344
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.960G>C
  hgvsp: ENST00000538587.1:c.960G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.429G>C
  hgvsp: ENST00000586553.1:c.429G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.327G>C
  hgvsp: ENST00000535384.1:c.327G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.840G>C
  hgvsp: ENST00000269185.4:c.840G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1182G>C
  hgvsp: ENST00000589544.1:c.1182G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1134G>C
  hgvsp: ENST00000590712.1:c.1134G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1182G>C
  hgvsp: ENST00000261592.5:c.1182G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.717G>C
  hgvsp: ENST00000535475.1:c.717G>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*791G>C
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2373
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3932
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Ser394Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: Other
population: Latino
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: MQ

18-31538257-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538257
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538257
    reference: chr 18
allele count: 5
allele frequency: 4.120516877637131e-5
allele num: 121344
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.840G>A
  hgvsp: ENST00000269185.4:c.840G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1182G>A
  hgvsp: ENST00000589544.1:c.1182G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1182G>A
  hgvsp: ENST00000261592.5:c.1182G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.717G>A
  hgvsp: ENST00000535475.1:c.717G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.429G>A
  hgvsp: ENST00000586553.1:c.429G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1134G>A
  hgvsp: ENST00000590712.1:c.1134G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.960G>A
  hgvsp: ENST00000538587.1:c.960G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.327G>A
  hgvsp: ENST00000535384.1:c.327G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*791G>A
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 364
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 8077
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7906
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6014
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10221
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2679
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Ser394Ser
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: European (Non-Finnish)
population: Latino
reference allele: C
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP

18-31538258-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538258
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538258
    reference: chr 18
allele count: 4
allele frequency: 3.296413502109704e-5
allele num: 121344
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.716C>T
  hgvsp: ENSP00000438190.1:p.Ser239Leu
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1181C>T
  hgvsp: ENSP00000465450.1:p.Ser394Leu
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.326C>T
  hgvsp: ENSP00000445733.1:p.Ser109Leu
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*790C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.839C>T
  hgvsp: ENSP00000269185.4:p.Ser280Leu
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1133C>T
  hgvsp: ENSP00000467629.1:p.Ser378Leu
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.959C>T
  hgvsp: ENSP00000443472.1:p.Ser320Leu
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1181C>T
  hgvsp: ENSP00000261592.4:p.Ser394Leu
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.428C>T
  hgvsp: ENSP00000467015.1:p.Ser143Leu
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7907
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8079
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9074
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6065
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 572
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10225
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 458
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6013
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 363
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4123
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 818
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1658
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1125
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2677
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ser394Leu
num of homozygotes: 0
population: African
population: European (Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

18-31538263-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538263
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538263
    reference: chr 18
allele count: 394
allele frequency: 3.246860269637736e-3
allele num: 121348
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1128C>T
  hgvsp: ENST00000590712.1:c.1128C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*785C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.954C>T
  hgvsp: ENST00000538587.1:c.954C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.711C>T
  hgvsp: ENST00000535475.1:c.711C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1176C>T
  hgvsp: ENST00000261592.5:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.834C>T
  hgvsp: ENST00000269185.4:c.834C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.321C>T
  hgvsp: ENST00000535384.1:c.321C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1176C>T
  hgvsp: ENST00000589544.1:c.1176C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.423C>T
  hgvsp: ENST00000586553.1:c.423C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 588
  bin: 7.75e1
  variant carriers: 22
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5995
  bin: 4.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 474
  bin: 8.25e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8045
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7882
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10193
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1133
  bin: 6.75e1
  variant carriers: 18
genotype depth: GenotypeDepth
  all individuals: 4112
  bin: 5.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 822
  bin: 7.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2667
  bin: 5.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 1399
  bin: 9.75e1
  variant carriers: 236
genotype depth: GenotypeDepth
  all individuals: 5931
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 330
  bin: 9.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 381
  bin: 8.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 9043
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1657
  bin: 6.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2362
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15336
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Asp392Asp
num of homozygotes: 13
population: African
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: East Asian
reference allele: G
site quality: FS
site quality: MQ
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: BaseQRankSum

18-31538266-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538266
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538266
    reference: chr 18
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.831T>C
  hgvsp: ENST00000269185.4:c.831T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.318T>C
  hgvsp: ENST00000535384.1:c.318T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*782T>C
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1173T>C
  hgvsp: ENST00000261592.5:c.1173T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1173T>C
  hgvsp: ENST00000589544.1:c.1173T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.708T>C
  hgvsp: ENST00000535475.1:c.708T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.951T>C
  hgvsp: ENST00000538587.1:c.951T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1125T>C
  hgvsp: ENST00000590712.1:c.1125T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.420T>C
  hgvsp: ENST00000586553.1:c.420T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10286
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2386
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.His391His
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: VQSLOD

18-31538267-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538267
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538267
    reference: chr 18
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.317A>G
  hgvsp: ENSP00000445733.1:p.His106Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1172A>G
  hgvsp: ENSP00000465450.1:p.His391Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.419A>G
  hgvsp: ENSP00000467015.1:p.His140Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.707A>G
  hgvsp: ENSP00000438190.1:p.His236Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.830A>G
  hgvsp: ENSP00000269185.4:p.His277Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1124A>G
  hgvsp: ENSP00000467629.1:p.His375Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1172A>G
  hgvsp: ENSP00000261592.4:p.His391Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.950A>G
  hgvsp: ENSP00000443472.1:p.His317Arg
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*781A>G
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 457
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10285
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5959
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8176
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 809
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6015
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.His391Arg
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: QD

18-31538273-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538273
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538273
    reference: chr 18
allele count: 1
allele frequency: 8.240626287597857e-6
allele num: 121350
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.311A>G
  hgvsp: ENSP00000445733.1:p.Glu104Gly
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1118A>G
  hgvsp: ENSP00000467629.1:p.Glu373Gly
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.944A>G
  hgvsp: ENSP00000443472.1:p.Glu315Gly
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*775A>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1166A>G
  hgvsp: ENSP00000465450.1:p.Glu389Gly
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.701A>G
  hgvsp: ENSP00000438190.1:p.Glu234Gly
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.413A>G
  hgvsp: ENSP00000467015.1:p.Glu138Gly
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.824A>G
  hgvsp: ENSP00000269185.4:p.Glu275Gly
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1166A>G
  hgvsp: ENSP00000261592.4:p.Glu389Gly
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10287
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 567
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5954
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9090
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7912
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8179
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6018
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22171
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Glu389Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Finnish)
reference allele: T
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: QD

18-31538274-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538274
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538274
    reference: chr 18
allele count: 4
allele frequency: 3.296359171295305e-5
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.823G>A
  hgvsp: ENSP00000269185.4:p.Glu275Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.943G>A
  hgvsp: ENSP00000443472.1:p.Glu315Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1165G>A
  hgvsp: ENSP00000465450.1:p.Glu389Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*774G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.310G>A
  hgvsp: ENSP00000445733.1:p.Glu104Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1117G>A
  hgvsp: ENSP00000467629.1:p.Glu373Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.700G>A
  hgvsp: ENSP00000438190.1:p.Glu234Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.412G>A
  hgvsp: ENSP00000467015.1:p.Glu138Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1165G>A
  hgvsp: ENSP00000261592.4:p.Glu389Lys
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8175
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5955
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7911
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1172
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4269
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Glu389Lys
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: African
population: South Asian
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP

18-31538280-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538280
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538280
    reference: chr 18
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1159G>A
  hgvsp: ENSP00000465450.1:p.Asp387Asn
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.406G>A
  hgvsp: ENSP00000467015.1:p.Asp136Asn
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.304G>A
  hgvsp: ENSP00000445733.1:p.Asp102Asn
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*768G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1159G>A
  hgvsp: ENSP00000261592.4:p.Asp387Asn
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.937G>A
  hgvsp: ENSP00000443472.1:p.Asp313Asn
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1111G>A
  hgvsp: ENSP00000467629.1:p.Asp371Asn
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.694G>A
  hgvsp: ENSP00000438190.1:p.Asp232Asn
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.817G>A
  hgvsp: ENSP00000269185.4:p.Asp273Asn
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 10288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 808
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9089
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5952
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 566
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15516
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Asp387Asn
num of homozygotes: 0
population: African
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: C
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

18-31538286-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538286
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538286
    reference: chr 18
allele count: 3
allele frequency: 2.472106399459433e-5
allele num: 121354
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.400G>A
  hgvsp: ENSP00000467015.1:p.Glu134Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1105G>A
  hgvsp: ENSP00000467629.1:p.Glu369Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.931G>A
  hgvsp: ENSP00000443472.1:p.Glu311Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1153G>A
  hgvsp: ENSP00000261592.4:p.Glu385Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1153G>A
  hgvsp: ENSP00000465450.1:p.Glu385Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.811G>A
  hgvsp: ENSP00000269185.4:p.Glu271Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.688G>A
  hgvsp: ENSP00000438190.1:p.Glu230Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.298G>A
  hgvsp: ENSP00000445733.1:p.Glu100Lys
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*762G>A
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10288
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1171
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8183
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7914
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4115
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 807
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1119
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6014
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Glu385Lys
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: Other
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ

18-31538287-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538287
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538287
    reference: chr 18
allele count: 14
allele frequency: 1.15363064042981e-4
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.297C>T
  hgvsp: ENST00000535384.1:c.297C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1152C>T
  hgvsp: ENST00000589544.1:c.1152C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1104C>T
  hgvsp: ENST00000590712.1:c.1104C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.930C>T
  hgvsp: ENST00000538587.1:c.930C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.687C>T
  hgvsp: ENST00000535475.1:c.687C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.810C>T
  hgvsp: ENST00000269185.4:c.810C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1152C>T
  hgvsp: ENST00000261592.5:c.1152C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*761C>T
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.399C>T
  hgvsp: ENST00000586553.1:c.399C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8182
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 9.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Asp384Asp
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: East Asian
population: Latino
population: African
reference allele: G
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: QD

18-31538287-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538287
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538287
    reference: chr 18
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*761C>G
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.810C>G
  hgvsp: ENSP00000269185.4:p.Asp270Glu
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.297C>G
  hgvsp: ENSP00000445733.1:p.Asp99Glu
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.687C>G
  hgvsp: ENSP00000438190.1:p.Asp229Glu
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1152C>G
  hgvsp: ENSP00000261592.4:p.Asp384Glu
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1152C>G
  hgvsp: ENSP00000465450.1:p.Asp384Glu
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1104C>G
  hgvsp: ENSP00000467629.1:p.Asp368Glu
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.930C>G
  hgvsp: ENSP00000443472.1:p.Asp310Glu
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.399C>G
  hgvsp: ENSP00000467015.1:p.Asp133Glu
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1183
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6006
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1118
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4111
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1652
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7913
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10289
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9087
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5949
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 564
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8182
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3938
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4269
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Asp384Glu
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

18-31538289-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 31538289
    reference: chr 18
  end: Position
    type: ExactPosition
    position: 31538289
    reference: chr 18
allele count: 1
allele frequency: 8.240897928238261e-6
allele num: 121346
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000464704
  ensembl transcript: ENST00000586314
  gene symbol: NOL4
  hgvsc: ENST00000586314.1:c.*759G>A
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467015
  ensembl transcript: ENST00000586553
  gene symbol: NOL4
  hgvsc: ENST00000586553.1:c.397G>A
  hgvsp: ENSP00000467015.1:p.Asp133Asn
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000467629
  ensembl transcript: ENST00000590712
  gene symbol: NOL4
  hgvsc: ENST00000590712.1:c.1102G>A
  hgvsp: ENSP00000467629.1:p.Asp368Asn
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000465450
  ensembl transcript: ENST00000589544
  gene symbol: NOL4
  hgvsc: ENST00000589544.1:c.1150G>A
  hgvsp: ENSP00000465450.1:p.Asp384Asn
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000269185
  ensembl transcript: ENST00000269185
  gene symbol: NOL4
  hgvsc: ENST00000269185.4:c.808G>A
  hgvsp: ENSP00000269185.4:p.Asp270Asn
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000445733
  ensembl transcript: ENST00000535384
  gene symbol: NOL4
  hgvsc: ENST00000535384.1:c.295G>A
  hgvsp: ENSP00000445733.1:p.Asp99Asn
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000438190
  ensembl transcript: ENST00000535475
  gene symbol: NOL4
  hgvsc: ENST00000535475.1:c.685G>A
  hgvsp: ENSP00000438190.1:p.Asp229Asn
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000443472
  ensembl transcript: ENST00000538587
  gene symbol: NOL4
  hgvsc: ENST00000538587.1:c.928G>A
  hgvsp: ENSP00000443472.1:p.Asp310Asn
  variant of: http://identifiers.org/hgnc/7870
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000101746
  ensembl protein: ENSP00000261592
  ensembl transcript: ENST00000261592
  gene symbol: NOL4
  hgvsc: ENST00000261592.5:c.1150G>A
  hgvsp: ENSP00000261592.4:p.Asp384Asn
  variant of: http://identifiers.org/hgnc/7870
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 8185
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 565
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10292
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9091
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5948
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 806
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1169
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6003
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7915
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4114
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 362
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Asp384Asn
num of homozygotes: 0
reference allele: C

GenotypeQuality
all individuals: 117
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 865
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 402
bin: 3.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8229
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 158
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 227
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35025
bin: 6.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

Latino
type: Population
allele count: 4
allele frequency: 3.675794890645102e-4
allele num: 10882
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 3.196249733645856e-4
allele num: 9386
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62830
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7908
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16028
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.435e0

MQRankSum
type: SiteQuality
SIO_000300: -4.08e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.828e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.7e-2

QD
type: SiteQuality
SIO_000300: 1.485e1

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

DP
type: SiteQuality
SIO_000300: 1.653376e6

GenotypeQuality
all individuals: 8229
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 35025
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 976
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6140
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 842
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2049
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 411
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 225
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 454
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1838
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1314
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 158
bin: 4.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.065416577881952e-4
allele num: 9386
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6456
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16028
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62830
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7908
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.7e-2

MQRankSum
type: SiteQuality
SIO_000300: -4.08e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.89e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.1e-3

FS
type: SiteQuality
SIO_000300: 4.435e0

DP
type: SiteQuality
SIO_000300: 1.653376e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.828e0

QD
type: SiteQuality
SIO_000300: 1.485e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.78e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

GenotypeQuality
all individuals: 405
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 302
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 304
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6222
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 34960
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 981
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1283
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 393
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 231
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1967
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 175
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 1744
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 232
bin: 4.75e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10846
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 864
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 62544
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9350
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16014
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6454
num of homozygotes: 0

East Asian
type: Population
allele count: 7
allele frequency: 8.935409752361502e-4
allele num: 7834
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 1.64e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.138e0

MQ
type: SiteQuality
SIO_000300: 5.924e1

VQSLOD
type: SiteQuality
SIO_000300: 6.929999999999999e-1

FS
type: SiteQuality
SIO_000300: 3.669e0

DP
type: SiteQuality
SIO_000300: 1.651351e6

MQRankSum
type: SiteQuality
SIO_000300: 2.48e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.57e-1

QD
type: SiteQuality
SIO_000300: 1.311e1

GenotypeQuality
all individuals: 1808
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 528
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 297
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 256
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 7438
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1106
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 348
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 388
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33494
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 345
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1244
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 861
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15880
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6434
num of homozygotes: 0

Latino
type: Population
allele count: 2
allele frequency: 1.86046511627907e-4
allele num: 10750
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.852641454498399e-5
allele num: 61822
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7738
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9214
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 1.617501e6

QD
type: SiteQuality
SIO_000300: 8.18e0

MQRankSum
type: SiteQuality
SIO_000300: 1.56e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.1e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.2e-2

FS
type: SiteQuality
SIO_000300: 1.1091e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

MQ
type: SiteQuality
SIO_000300: 6.077e1

GenotypeQuality
all individuals: 288
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 183
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2107
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1200
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 902
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2053
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 197
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 818
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 30340
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 248
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5608
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 301
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 636
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 11007
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7484
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8984
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 842
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.650764303872693e-5
allele num: 60578
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10528
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15706
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6354
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.582e0

ClippingRankSum
type: SiteQuality
SIO_000300: 6.16e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.305e0

DP
type: SiteQuality
SIO_000300: 1.480722e6

QD
type: SiteQuality
SIO_000300: 1.209e1

MQRankSum
type: SiteQuality
SIO_000300: 1.16e-1

FS
type: SiteQuality
SIO_000300: 3.274e0

VQSLOD
type: SiteQuality
SIO_000300: -1.497e-1

MQ
type: SiteQuality
SIO_000300: 5.942e1

GenotypeQuality
all individuals: 615
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2185
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 185
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 288
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2210
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 216
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 829
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30696
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5458
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 181
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1060
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1065
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 418
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 11647
bin: 2.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 840
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 60458
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7450
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8976
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.375111564452378e-5
allele num: 15686
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6350
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10516
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.699e0

DP
type: SiteQuality
SIO_000300: 1.449004e6

FS
type: SiteQuality
SIO_000300: 2.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.3e-3

QD
type: SiteQuality
SIO_000300: 9.550000000000001e0

MQRankSum
type: SiteQuality
SIO_000300: -1.37e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.93e-1

MQ
type: SiteQuality
SIO_000300: 5.946e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.8e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -4.9e-1

GenotypeQuality
all individuals: 977
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3039
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 280
bin: 9.25e1
variant carriers: 1

GenotypeQuality
all individuals: 380
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4743
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 265
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1496
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3320
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26341
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 585
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 274
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 237
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1060
bin: 9.75e1
variant carriers: 7

GenotypeQuality
all individuals: 399
bin: 4.25e1
variant carriers: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8778
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7232
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.424257998201208e-5
allele num: 15566
num of homozygotes: 0

European (Non-Finnish)
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allele count: 6
allele frequency: 1.010339137170377e-4
allele num: 59386
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 9.688044952528579e-5
allele num: 10322
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6280
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.357265e6

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.997e1

ClippingRankSum
type: SiteQuality
SIO_000300: 2.89e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 2.3e0

InbreedingCoeff
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SIO_000300: -3.3e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.21e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.89e-1

QD
type: SiteQuality
SIO_000300: 1.129e1

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 6874
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15350
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8480
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6210
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 814
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10054
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.740219963803425e-5
allele num: 57464
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.01e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.06e-1

DP
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
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SIO_000300: -8.03e-1

InbreedingCoeff
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.11e-1

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 8.26e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 0.0e0
allele num: 6440
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 14992
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8004
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6066
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.836344939033348e-5
allele num: 54456
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9594
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 3.96e-1

DP
type: SiteQuality
SIO_000300: 1.041115e6

ReadPosRankSum
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SIO_000300: 1.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.855e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-2

MQ
type: SiteQuality
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MQRankSum
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SIO_000300: -7.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.524e0

QD
type: SiteQuality
SIO_000300: 1.488e1

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9594
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6066
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 54456
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 8004
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.552795031055901e-4
allele num: 6440
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14992
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.041115e6

VQSLOD
type: SiteQuality
SIO_000300: 3.96e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.16e0

MQRankSum
type: SiteQuality
SIO_000300: -7.02e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.524e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.855e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.488e1

GenotypeQuality
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variant carriers: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 11476
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10266
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.549666821633349e-5
allele num: 64530
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 828
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6570
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8460
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BaseQRankSum
type: SiteQuality
SIO_000300: -3.285e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.26e-1

MQ
type: SiteQuality
SIO_000300: 5.927e1

MQRankSum
type: SiteQuality
SIO_000300: -2.004e0

QD
type: SiteQuality
SIO_000300: 1.001e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.76e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.4e-3

DP
type: SiteQuality
SIO_000300: 1.586451e6

VQSLOD
type: SiteQuality
SIO_000300: -1.668e0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11392
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11774
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8498
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10274
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.545499505440158e-5
allele num: 64704
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 830
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.03e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.3e-3

VQSLOD
type: SiteQuality
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DP
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.508e1

MQ
type: SiteQuality
SIO_000300: 5.866e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.15e-1

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.72951936174353e-5
allele num: 10278
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 64742
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8518
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11838
num of homozygotes: 0

Other
type: Population
allele count: 0
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MQRankSum
type: SiteQuality
SIO_000300: 2.2e-1

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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MQ
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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FS
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VQSLOD
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6582
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
allele num: 11404
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South Asian
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num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.72951936174353e-5
allele num: 10278
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 6.178369528281487e-5
allele num: 64742
num of homozygotes: 0

East Asian
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Other
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ClippingRankSum
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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MQRankSum
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FS
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MQ
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BaseQRankSum
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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num of homozygotes: 0

African
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South Asian
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European (Non-Finnish)
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allele frequency: 4.625489530975362e-5
allele num: 64858
num of homozygotes: 0

Latino
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Other
type: Population
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European (Finnish)
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ClippingRankSum
type: SiteQuality
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MQRankSum
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FS
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QD
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VQSLOD
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BaseQRankSum
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MQ
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DP
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InbreedingCoeff
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

African
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allele frequency: 0.0e0
allele num: 10398
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.506296318611797e-5
allele num: 66388
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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Other
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allele count: 0
allele frequency: 0.0e0
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ClippingRankSum
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.0925e1

QD
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BaseQRankSum
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SIO_000300: -7.79e-1

InbreedingCoeff
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VQSLOD
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MQRankSum
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DP
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 8.682062858135092e-5
allele num: 11518
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European (Finnish)
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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East Asian
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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ClippingRankSum
type: SiteQuality
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VQSLOD
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InbreedingCoeff
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QD
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DP
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MQRankSum
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ReadPosRankSum
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FS
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MQ
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BaseQRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502313562886846e-5
allele num: 66564
num of homozygotes: 0

South Asian
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allele num: 16470
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Latino
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allele count: 1
allele frequency: 8.685079034219212e-5
allele num: 11514
num of homozygotes: 0

African
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allele count: 1
allele frequency: 9.615384615384615e-5
allele num: 10400
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Other
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East Asian
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allele count: 0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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FS
type: SiteQuality
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QD
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
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BaseQRankSum
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DP
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MQRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele num: 11514
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Finnish)
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
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allele num: 66564
num of homozygotes: 0

Other
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FS
type: SiteQuality
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DP
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InbreedingCoeff
type: SiteQuality
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MQ
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QD
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MQRankSum
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ClippingRankSum
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ReadPosRankSum
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BaseQRankSum
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VQSLOD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66600
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African
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Latino
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European (Finnish)
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Other
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East Asian
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South Asian
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DP
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MQ
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FS
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QD
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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BaseQRankSum
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MQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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European (Finnish)
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European (Non-Finnish)
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Other
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East Asian
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Latino
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MQRankSum
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ReadPosRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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QD
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FS
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VQSLOD
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DP
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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Latino
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African
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European (Finnish)
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East Asian
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South Asian
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ReadPosRankSum
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MQRankSum
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QD
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FS
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DP
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MQ
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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Other
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European (Finnish)
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Latino
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South Asian
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East Asian
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allele frequency: 0.0e0
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66616
num of homozygotes: 0

InbreedingCoeff
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VQSLOD
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FS
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MQ
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BaseQRankSum
type: SiteQuality
SIO_000300: -9.69e-1

MQRankSum
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SIO_000300: -2.02e-1

QD
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ClippingRankSum
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SIO_000300: 7.11e-1

ReadPosRankSum
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DP
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SIO_000300: 1.679257e6

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16460
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.506114826194349e-5
allele num: 66396
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10362
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8486
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6554
num of homozygotes: 0

VQSLOD
type: SiteQuality
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ReadPosRankSum
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QD
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DP
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InbreedingCoeff
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SIO_000300: -4.0e-4

FS
type: SiteQuality
SIO_000300: 4.779e0

BaseQRankSum
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MQ
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SIO_000300: 5.939e1

MQRankSum
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SIO_000300: 1.02e0

ClippingRankSum
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SIO_000300: 5.26e-1

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66062
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10340
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6524
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8438
num of homozygotes: 0

Latino
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allele count: 1
allele frequency: 8.815232722143864e-5
allele num: 11344
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e0

ClippingRankSum
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SIO_000300: -1.382e0

MQRankSum
type: SiteQuality
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DP
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SIO_000300: 1.657766e6

InbreedingCoeff
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BaseQRankSum
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SIO_000300: -1.15e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.918e0

FS
type: SiteQuality
SIO_000300: 3.702e0

MQ
type: SiteQuality
SIO_000300: 5.796e1

QD
type: SiteQuality
SIO_000300: 1.541e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 30

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 30
allele frequency: 4.56093407929944e-4
allele num: 65776
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6508
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10294
num of homozygotes: 0

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8404
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16136
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11282
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.582e0

MQRankSum
type: SiteQuality
SIO_000300: 1.58e-1

DP
type: SiteQuality
SIO_000300: 1.641637e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e-1

MQ
type: SiteQuality
SIO_000300: 5.963e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.4e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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SIO_000300: 3.7e0

QD
type: SiteQuality
SIO_000300: 1.257e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6436
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11142
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8238
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10124
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15586
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.546264225630876e-5
allele num: 64672
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.7e-1

MQ
type: SiteQuality
SIO_000300: 5.956e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.29e-1

ReadPosRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.582265e6

InbreedingCoeff
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SIO_000300: 3.5e-3

BaseQRankSum
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SIO_000300: -1.967e0

QD
type: SiteQuality
SIO_000300: 1.212e1

FS
type: SiteQuality
SIO_000300: 1.917e0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 14660
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9810
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.59311773140035e-5
allele num: 62770
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 60368
num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele frequency: 2.626050420168067e-4
allele num: 7616
num of homozygotes: 0

South Asian
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BaseQRankSum
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DP
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VQSLOD
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MQRankSum
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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FS
type: SiteQuality
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MQ
type: SiteQuality
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
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African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.707766923970216e-5
allele num: 58556
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Latino
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European (Finnish)
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South Asian
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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DP
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VQSLOD
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FS
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MQ
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InbreedingCoeff
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QD
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
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East Asian
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.770977225232884e-5
allele num: 56466
num of homozygotes: 0

Other
type: Population
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num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 9560
num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
allele num: 5870
num of homozygotes: 0

MQ
type: SiteQuality
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DP
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BaseQRankSum
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MQRankSum
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FS
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InbreedingCoeff
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VQSLOD
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QD
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1026
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 249
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4135
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2144
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4237
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3902
bin: 9.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11448
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8514
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14502
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 1.931247585940518e-4
allele num: 10356
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65782
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 6.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.41e0

QD
type: SiteQuality
SIO_000300: 1.464e1

MQ
type: SiteQuality
SIO_000300: 5.987e1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.8e-1

FS
type: SiteQuality
SIO_000300: 5.478e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.39e-1

MQRankSum
type: SiteQuality
SIO_000300: 7.9e-1

DP
type: SiteQuality
SIO_000300: 2.468215e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-2

GenotypeQuality
all individuals: 22651
bin: 9.75e1
variant carriers: 205

GenotypeQuality
all individuals: 1006
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1369
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2309
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 102
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 547
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10056
bin: 6.25e1
variant carriers: 1

GenotypeQuality
all individuals: 4106
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 132
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 168
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2143
bin: 8.75e1
variant carriers: 3

GenotypeQuality
all individuals: 3893
bin: 9.25e1
variant carriers: 5

GenotypeQuality
all individuals: 4205
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 38
allele frequency: 2.630850180005539e-3
allele num: 14444
num of homozygotes: 0

Latino
type: Population
allele count: 21
allele frequency: 1.834702079329023e-3
allele num: 11446
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8506
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 143
allele frequency: 2.175037264624464e-3
allele num: 65746
num of homozygotes: 1

European (Finnish)
type: Population
allele count: 2
allele frequency: 3.03030303030303e-4
allele num: 6600
num of homozygotes: 0

African
type: Population
allele count: 10
allele frequency: 9.656237929702588e-4
allele num: 10356
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.1441647597254e-3
allele num: 874
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.2e-2

MQRankSum
type: SiteQuality
SIO_000300: 2.75e-1

QD
type: SiteQuality
SIO_000300: 1.398e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.86e-2

VQSLOD
type: SiteQuality
SIO_000300: 6.35e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.77e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 2.471483e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.696e0

GenotypeQuality
all individuals: 437
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 109
bin: 1.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 689
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2310
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 865
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variant carriers: 0

GenotypeQuality
all individuals: 4108
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variant carriers: 0

GenotypeQuality
all individuals: 128
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10453
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4216
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22496
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3904
bin: 9.25e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10356
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.521005080156968e-5
allele num: 65746
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11444
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14478
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 1.3617e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.58e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.596e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.3e-2

VQSLOD
type: SiteQuality
SIO_000300: -2.058e0

QD
type: SiteQuality
SIO_000300: 2.89e0

DP
type: SiteQuality
SIO_000300: 2.470917e6

MQRankSum
type: SiteQuality
SIO_000300: 2.0e-1

MQ
type: SiteQuality
SIO_000300: 5.947e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

GenotypeQuality
all individuals: 5586
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 857
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 48
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variant carriers: 0

GenotypeQuality
all individuals: 1442
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GenotypeQuality
all individuals: 4105
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variant carriers: 0

GenotypeQuality
all individuals: 102
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GenotypeQuality
all individuals: 164
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variant carriers: 0

GenotypeQuality
all individuals: 693
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variant carriers: 0

GenotypeQuality
all individuals: 83
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variant carriers: 0

GenotypeQuality
all individuals: 359
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GenotypeQuality
all individuals: 22497
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variant carriers: 1

GenotypeQuality
all individuals: 10674
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variant carriers: 0

GenotypeQuality
all individuals: 3904
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 376
bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.519895431194334e-5
allele num: 65794
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8516
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 14646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10358
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 2.472867e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.27e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.03e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.900000000000001e-3

VQSLOD
type: SiteQuality
SIO_000300: -1.881e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -4.65e-1

QD
type: SiteQuality
SIO_000300: 1.376e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.906e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.592e0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 3899
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4222
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variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2149
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variant carriers: 0

GenotypeQuality
all individuals: 4111
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variant carriers: 0

GenotypeQuality
all individuals: 332
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variant carriers: 0

GenotypeQuality
all individuals: 597
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variant carriers: 0

GenotypeQuality
all individuals: 12711
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2318
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variant carriers: 0

GenotypeQuality
all individuals: 22508
bin: 9.75e1
variant carriers: 69

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1210
bin: 2.25e1
variant carriers: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8570
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15076
num of homozygotes: 0

Latino
type: Population
allele count: 5
allele frequency: 4.35691878703381e-4
allele num: 11476
num of homozygotes: 0

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

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

African
type: Population
allele count: 55
allele frequency: 5.302738141149248e-3
allele num: 10372
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 10
allele frequency: 1.515932450050026e-4
allele num: 65966
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.976e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.869e0

VQSLOD
type: SiteQuality
SIO_000300: 3.41e0

QD
type: SiteQuality
SIO_000300: 1.448e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

FS
type: SiteQuality
SIO_000300: 9.389999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

DP
type: SiteQuality
SIO_000300: 2.496906e6

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

GenotypeQuality
all individuals: 4222
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 45
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3899
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4111
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 112
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2318
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2149
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
all individuals: 454
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variant carriers: 0

GenotypeQuality
all individuals: 597
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 78
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variant carriers: 0

GenotypeQuality
all individuals: 12711
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 1.25e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15076
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.166861143523921e-4
allele num: 8570
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 4.2e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.17e-2

FS
type: SiteQuality
SIO_000300: 9.389999999999999e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.99e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.869e0

VQSLOD
type: SiteQuality
SIO_000300: 3.41e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.82e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

QD
type: SiteQuality
SIO_000300: 1.448e1

DP
type: SiteQuality
SIO_000300: 2.496906e6

GenotypeQuality
all individuals: 89
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 437
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 91
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4118
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 563
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 83
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3904
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2153
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1161
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5711
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12888
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4229
bin: 8.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15190
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10376
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.515151515151515e-5
allele num: 66000
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11482
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8568
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.19e-1

VQSLOD
type: SiteQuality
SIO_000300: -2.666e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.415e0

ClippingRankSum
type: SiteQuality
SIO_000300: -6.38e-1

QD
type: SiteQuality
SIO_000300: 1.402e1

DP
type: SiteQuality
SIO_000300: 2.495203e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.749e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.9e-3

MQ
type: SiteQuality
SIO_000300: 5.93e1

GenotypeQuality
all individuals: 229
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 5.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 98
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 7.5e0
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GenotypeQuality
all individuals: 5750
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 412
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3905
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 331
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2327
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22464
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 4231
bin: 8.25e1
variant carriers: 0

African
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: 888
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15408
num of homozygotes: 0

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

Latino
type: Population
allele count: 2
allele frequency: 1.73973556019485e-4
allele num: 11496
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 7.571e0

DP
type: SiteQuality
SIO_000300: 2.502155e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 1.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 8.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -6.292e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.0e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.93e-1

QD
type: SiteQuality
SIO_000300: 1.386e1

GenotypeQuality
all individuals: 4229
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 30
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 124
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 105
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22
bin: 1.25e1
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 82
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13633
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 775
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5777
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3906
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.510254628930438e-5
allele num: 66214
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

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

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10384
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.509465e6

QD
type: SiteQuality
SIO_000300: 1.032e1

MQ
type: SiteQuality
SIO_000300: 5.979e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.31e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.5e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.38e0

MQRankSum
type: SiteQuality
SIO_000300: 7.92e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 8.9e-1

GenotypeQuality
all individuals: 14065
bin: 6.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 4.25e1
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GenotypeQuality
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bin: 5.25e1
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4229
bin: 8.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11506
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: 0
allele frequency: 0.0e0
allele num: 66308
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15854
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: 10392
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.163602513381429e-4
allele num: 8594
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 1.576e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.3e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.028e0

VQSLOD
type: SiteQuality
SIO_000300: 7.47e-1

MQRankSum
type: SiteQuality
SIO_000300: -8.1e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.06e0

FS
type: SiteQuality
SIO_000300: 2.487e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.598e0

DP
type: SiteQuality
SIO_000300: 2.513239e6

GenotypeQuality
all individuals: 102
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variant carriers: 0

GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 1

GenotypeQuality
all individuals: 80
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2151
bin: 8.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.508204633204633e-5
allele num: 66304
num of homozygotes: 0

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8592
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 15908
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 4.619e1

DP
type: SiteQuality
SIO_000300: 2.514261e6

VQSLOD
type: SiteQuality
SIO_000300: -1.163e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

QD
type: SiteQuality
SIO_000300: 5.9e-1

MQ
type: SiteQuality
SIO_000300: 5.177e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.16e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.097e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.619e0

MQRankSum
type: SiteQuality
SIO_000300: -3.94e-1

GenotypeQuality
all individuals: 58
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 144
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variant carriers: 0

GenotypeQuality
all individuals: 22456
bin: 9.75e1
variant carriers: 1

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

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16016
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8600
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66352
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.517222e6

QD
type: SiteQuality
SIO_000300: 1.35e1

MQRankSum
type: SiteQuality
SIO_000300: 1.87e-1

MQ
type: SiteQuality
SIO_000300: 5.986e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.07e0

FS
type: SiteQuality
SIO_000300: 1.987e0

BaseQRankSum
type: SiteQuality
SIO_000300: -6.432e0

VQSLOD
type: SiteQuality
SIO_000300: 2.68e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.42e-1

GenotypeQuality
all individuals: 171
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4239
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 35
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 3913
bin: 9.25e1
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GenotypeQuality
all individuals: 35
bin: 3.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10402
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66566
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: 904
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 2.530321e6

ClippingRankSum
type: SiteQuality
SIO_000300: -7.14e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

QD
type: SiteQuality
SIO_000300: 1.327e1

MQ
type: SiteQuality
SIO_000300: 5.952e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

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

GenotypeQuality
all individuals: 38
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 22458
bin: 9.75e1
variant carriers: 12

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8610
num of homozygotes: 0

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

African
type: Population
allele count: 12
allele frequency: 1.15362430301865e-3
allele num: 10402
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: 16420
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66566
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 2.25e0

BaseQRankSum
type: SiteQuality
SIO_000300: 4.06e0

MQRankSum
type: SiteQuality
SIO_000300: -1.06e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.14e-1

MQ
type: SiteQuality
SIO_000300: 5.952e1

QD
type: SiteQuality
SIO_000300: 1.327e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.05e0

DP
type: SiteQuality
SIO_000300: 2.530321e6

GenotypeQuality
all individuals: 3906
bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 29
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 11
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variant carriers: 0

GenotypeQuality
all individuals: 22510
bin: 9.75e1
variant carriers: 293

European (Non-Finnish)
type: Population
allele count: 215
allele frequency: 3.228228228228228e-3
allele num: 66600
num of homozygotes: 1

Latino
type: Population
allele count: 2
allele frequency: 1.73370319001387e-4
allele num: 11536
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.883506343713956e-4
allele num: 10404
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 29
allele frequency: 4.385964912280702e-3
allele num: 6612
num of homozygotes: 0

South Asian
type: Population
allele count: 45
allele frequency: 2.732572261355356e-3
allele num: 16468
num of homozygotes: 1

QD
type: SiteQuality
SIO_000300: 1.471e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 2.02e0

DP
type: SiteQuality
SIO_000300: 2.556222e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.47e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.6e-3

MQ
type: SiteQuality
SIO_000300: 5.976e1

MQRankSum
type: SiteQuality
SIO_000300: 3.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.07e0

FS
type: SiteQuality
SIO_000300: 0.0e0

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.071645415907711e-5
allele num: 16470
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66610
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8612
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -7.97e-1

QD
type: SiteQuality
SIO_000300: 2.105e1

VQSLOD
type: SiteQuality
SIO_000300: -1.837e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.661e0

ClippingRankSum
type: SiteQuality
SIO_000300: -9.1e-2

MQ
type: SiteQuality
SIO_000300: 6.0e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.91e-1

DP
type: SiteQuality
SIO_000300: 2.527731e6

GenotypeQuality
all individuals: 2360
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 21
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
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GenotypeQuality
all individuals: 15
bin: 7.5e0
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GenotypeQuality
all individuals: 2
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GenotypeQuality
all individuals: 15262
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GenotypeQuality
all individuals: 4258
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variant carriers: 0

GenotypeQuality
all individuals: 22334
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2162
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GenotypeQuality
all individuals: 3929
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 13
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variant carriers: 0

GenotypeQuality
all individuals: 3
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variant carriers: 0

GenotypeQuality
all individuals: 127
bin: 2.25e1
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GenotypeQuality
all individuals: 19
bin: 2.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 18
bin: 5.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.068697657482704e-5
allele num: 16478
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66608
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8616
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: 8.3e-1

DP
type: SiteQuality
SIO_000300: 2.528079e6

QD
type: SiteQuality
SIO_000300: 2.086e1

VQSLOD
type: SiteQuality
SIO_000300: -2.102e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.894e0

ClippingRankSum
type: SiteQuality
SIO_000300: 3.04e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.59e-1

FS
type: SiteQuality
SIO_000300: 9.65e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

GenotypeQuality
all individuals: 4254
bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 100
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2364
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 16
bin: 2.75e1
variant carriers: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159554730983302e-4
allele num: 8624
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 2
allele frequency: 1.73370319001387e-4
allele num: 11536
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.27e0

MQ
type: SiteQuality
SIO_000300: 5.95e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.322e0

FS
type: SiteQuality
SIO_000300: 4.41e0

VQSLOD
type: SiteQuality
SIO_000300: 1.8e0

QD
type: SiteQuality
SIO_000300: 1.347e1

DP
type: SiteQuality
SIO_000300: 2.528944e6

MQRankSum
type: SiteQuality
SIO_000300: 1.79e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -7.2e-1

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

GenotypeQuality
all individuals: 4
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
all individuals: 2
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variant carriers: 0

South Asian
type: Population
allele count: 29
allele frequency: 1.757575757575757e-3
allele num: 16500
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 90
allele frequency: 1.35041862977523e-3
allele num: 66646
num of homozygotes: 1

Latino
type: Population
allele count: 15
allele frequency: 1.299826689774697e-3
allele num: 11540
num of homozygotes: 0

Other
type: Population
allele count: 1
allele frequency: 1.103752759381898e-3
allele num: 906
num of homozygotes: 0

African
type: Population
allele count: 5
allele frequency: 4.805843906189927e-4
allele num: 10404
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 2.542231e6

MQRankSum
type: SiteQuality
SIO_000300: 2.6e-1

QD
type: SiteQuality
SIO_000300: 1.374e1

BaseQRankSum
type: SiteQuality
SIO_000300: 9.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.6e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.909999999999999e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.57e0

FS
type: SiteQuality
SIO_000300: 5.95e-1

MQ
type: SiteQuality
SIO_000300: 5.976e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.0e-2

GenotypeQuality
all individuals: 2170
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 6

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 4170
bin: 7.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 6.001140216641162e-5
allele num: 66654
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06060606060606e-5
allele num: 16500
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.954e1

VQSLOD
type: SiteQuality
SIO_000300: 2.27e0

DP
type: SiteQuality
SIO_000300: 2.528589e6

MQRankSum
type: SiteQuality
SIO_000300: -4.4e-2

FS
type: SiteQuality
SIO_000300: 1.262e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.347e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.24e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.71e-1

GenotypeQuality
all individuals: 10
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variant carriers: 0

GenotypeQuality
all individuals: 9
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variant carriers: 0

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

GenotypeQuality
all individuals: 5989
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3933
bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.499775011249437e-5
allele num: 66670
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
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: 906
num of homozygotes: 0

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

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

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

ClippingRankSum
type: SiteQuality
SIO_000300: -8.43e-1

MQRankSum
type: SiteQuality
SIO_000300: -4.9e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

DP
type: SiteQuality
SIO_000300: 2.528851e6

BaseQRankSum
type: SiteQuality
SIO_000300: -3.672e0

FS
type: SiteQuality
SIO_000300: 3.937e0

QD
type: SiteQuality
SIO_000300: 1.34e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 5989
bin: 6.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66670
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11558
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.937e0

DP
type: SiteQuality
SIO_000300: 2.528851e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.672e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.84e0

QD
type: SiteQuality
SIO_000300: 1.34e1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.43e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.43e0

MQRankSum
type: SiteQuality
SIO_000300: -4.9e-2

GenotypeQuality
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bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.49934029027228e-5
allele num: 66696
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
SIO_000300: 6.13e-1

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.275e1

ClippingRankSum
type: SiteQuality
SIO_000300: -4.79e-1

MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 9.51e-1

DP
type: SiteQuality
SIO_000300: 2.529031e6

MQ
type: SiteQuality
SIO_000300: 5.96e1

FS
type: SiteQuality
SIO_000300: 1.94e0

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

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

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.058403004967891e-5
allele num: 16506
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66696
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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VQSLOD
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.529031e6

MQRankSum
type: SiteQuality
SIO_000300: 1.5e0

BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.96e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
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GenotypeQuality
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bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2373
bin: 7.25e1
variant carriers: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
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: 1
allele frequency: 6.056201550387597e-5
allele num: 16512
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66704
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: -9.311e-1

MQRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 2.528958e6

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 3.963e0

QD
type: SiteQuality
SIO_000300: 1.137e1

GenotypeQuality
all individuals: 22278
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2170
bin: 8.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 1.75e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

FS
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SIO_000300: 3.445e0

BaseQRankSum
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SIO_000300: 2.14e0

ReadPosRankSum
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SIO_000300: 1.78e0

MQRankSum
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ClippingRankSum
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InbreedingCoeff
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SIO_000300: 0.0e0

QD
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DP
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SIO_000300: 2.529868e6

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.961e1

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

European (Finnish)
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allele count: 1
allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

South Asian
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allele count: 3
allele frequency: 1.816860465116279e-4
allele num: 16512
num of homozygotes: 0

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

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

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

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

FS
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.961e1

ClippingRankSum
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ReadPosRankSum
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QD
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BaseQRankSum
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VQSLOD
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InbreedingCoeff
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SIO_000300: 0.0e0

MQRankSum
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SIO_000300: -2.43e-1

DP
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SIO_000300: 2.529868e6

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

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

South Asian
type: Population
allele count: 4
allele frequency: 2.422480620155039e-4
allele num: 16512
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66710
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 9.68e-1

FS
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SIO_000300: 0.0e0

ReadPosRankSum
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QD
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InbreedingCoeff
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MQ
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MQRankSum
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DP
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SIO_000300: 2.529674e6

BaseQRankSum
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SIO_000300: 1.14e0

ClippingRankSum
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SIO_000300: -9.55e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 381

GenotypeQuality
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African
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allele count: 3
allele frequency: 2.883506343713956e-4
allele num: 10404
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 16
allele frequency: 2.398369109005876e-4
allele num: 66712
num of homozygotes: 0

Latino
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allele count: 13
allele frequency: 1.124372945857118e-3
allele num: 11562
num of homozygotes: 0

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

South Asian
type: Population
allele count: 358
allele frequency: 2.16812015503876e-2
allele num: 16512
num of homozygotes: 13

Other
type: Population
allele count: 3
allele frequency: 3.303964757709251e-3
allele num: 908
num of homozygotes: 0

East Asian
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allele count: 1
allele frequency: 1.157943492357573e-4
allele num: 8636
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.46e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.89e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.16e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.44e0

MQRankSum
type: SiteQuality
SIO_000300: 3.87e-1

DP
type: SiteQuality
SIO_000300: 2.565553e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.12e-2

QD
type: SiteQuality
SIO_000300: 1.33e1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.09e0

GenotypeQuality
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variant carriers: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11560
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498980693128672e-5
allele num: 66712
num of homozygotes: 0

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

African
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8636
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
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BaseQRankSum
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SIO_000300: -1.145e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.77e-1

MQRankSum
type: SiteQuality
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ClippingRankSum
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DP
type: SiteQuality
SIO_000300: 2.528223e6

QD
type: SiteQuality
SIO_000300: 1.352e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 3.342e0

MQ
type: SiteQuality
SIO_000300: 5.98e1

VQSLOD
type: SiteQuality
SIO_000300: 4.04e-1

GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66714
num of homozygotes: 0

South Asian
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allele frequency: 6.056201550387597e-5
allele num: 16512
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African
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allele frequency: 0.0e0
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele count: 0
allele frequency: 0.0e0
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Other
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BaseQRankSum
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FS
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MQ
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SIO_000300: 6.0e1

InbreedingCoeff
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VQSLOD
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ClippingRankSum
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MQRankSum
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ReadPosRankSum
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DP
type: SiteQuality
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QD
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SIO_000300: 1.05e1

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

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

African
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allele frequency: 0.0e0
allele num: 10404
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South Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

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

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

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

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

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

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

European (Non-Finnish)
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allele count: 3
allele frequency: 4.496807266840543e-5
allele num: 66714
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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African
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allele frequency: 9.611687812379854e-5
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South Asian
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BaseQRankSum
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QD
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ClippingRankSum
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MQ
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MQRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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FS
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 6015
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3939
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4170
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 22171
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10404
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: 11566
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

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

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

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -2.445e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.14e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -5.826e0

MQ
type: SiteQuality
SIO_000300: 5.931e1

MQRankSum
type: SiteQuality
SIO_000300: -6.39e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.649999999999999e-1

DP
type: SiteQuality
SIO_000300: 2.528307e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 0.0e0

QD
type: SiteQuality
SIO_000300: 4.18e0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3940
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 15516
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5
bin: 3.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 22171
bin: 9.75e1
variant carriers: 3

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

GenotypeQuality
all individuals: 4172
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4270
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2385
bin: 7.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 2172
bin: 8.75e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498890820792613e-5
allele num: 66716
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11562
num of homozygotes: 0

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

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

MQRankSum
type: SiteQuality
SIO_000300: 6.900000000000001e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.13e-1

DP
type: SiteQuality
SIO_000300: 2.528891e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

QD
type: SiteQuality
SIO_000300: 1.25e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.293e0

VQSLOD
type: SiteQuality
SIO_000300: 4.07e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.88e0

MQ
type: SiteQuality
SIO_000300: 5.949e1

GenotypeQuality
all individuals: 2384
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6014
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 4269
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 4170
bin: 7.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 22174
bin: 9.75e1
variant carriers: 14

GenotypeQuality
all individuals: 15516
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3938
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 13
allele frequency: 1.948558067030398e-4
allele num: 66716
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

MQRankSum
type: SiteQuality
SIO_000300: -2.81e-1

DP
type: SiteQuality
SIO_000300: 2.531289e6

QD
type: SiteQuality
SIO_000300: 1.342e1

GenotypeQuality
all individuals: 4170
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2171
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 33
bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 15516
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 8
bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
all individuals: 22174
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 6
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 3
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6014
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 4
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2384
bin: 7.25e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16512
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: 10404
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11566
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.157675387821255e-4
allele num: 8638
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66716
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -2.81e-1

MQ
type: SiteQuality
SIO_000300: 5.959e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

DP
type: SiteQuality
SIO_000300: 2.531289e6

QD
type: SiteQuality
SIO_000300: 1.342e1

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.17e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.07e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.51e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.77e0