4-142053993-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142053993
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142053993
    reference: chr 4
allele count: 1
allele frequency: 1.088921314545811e-5
allele num: 91834
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170153
  ensembl protein: ENSP00000425840
  ensembl transcript: ENST00000515673
  gene symbol: RNF150
  hgvsc: ENST00000515673.2:c.-31G>A
  variant of: http://identifiers.org/hgnc/23138
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000170153
  ensembl protein: ENSP00000394581
  ensembl transcript: ENST00000420921
  gene symbol: RNF150
  hgvsc: ENST00000420921.2:c.-5-79108G>A
  variant of: http://identifiers.org/hgnc/23138
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170153
  ensembl protein: ENSP00000425568
  ensembl transcript: ENST00000507500
  gene symbol: RNF150
  hgvsc: ENST00000507500.1:c.-31G>A
  variant of: http://identifiers.org/hgnc/23138
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000170153
  ensembl protein: ENSP00000304321
  ensembl transcript: ENST00000306799
  gene symbol: RNF150
  hgvsc: ENST00000306799.3:c.-31G>A
  variant of: http://identifiers.org/hgnc/23138
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3757
  bin: 2.5e0
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1498
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5701
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11104
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 21470
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7706
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 48
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6850
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 245
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1594
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 341
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 325
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1536
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 264
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 113
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23849
  bin: 2.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 661
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4043
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 510
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 648
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 248
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: African
reference allele: C
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: FS
site quality: DP
site quality: ClippingRankSum

4-142143477-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143477
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143477
    reference: chr 4
allele count: 1
allele frequency: 8.871382693706642e-6
allele num: 112722
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.-6-43A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.-6-43A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-115-43A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.-6-43A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.-6-43A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.-6-43A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.223-43A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.-6-43A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.-6-43A>G
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 13687
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13329
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3832
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1868
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11649
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7819
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4203
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5064
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 12213
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2977
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: A
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-142143480-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143480
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143480
    reference: chr 4
allele count: 1
allele frequency: 8.874374356607859e-6
allele num: 112684
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.-6-40C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.-6-40C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.-6-40C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-115-40C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.-6-40C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.-6-40C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.-6-40C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.-6-40C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.223-40C>T
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7926
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3812
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3645
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12112
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 404
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14791
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  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1874
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11616
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1156
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 768
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5192
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1855
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2644
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2953
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3049
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
population: African
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD

4-142143493-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143493
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143493
    reference: chr 4
allele count: 3
allele frequency: 2.651910259356823e-5
allele num: 113126
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.-6-27C>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.-6-27C>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.-6-27C>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.223-27C>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.-6-27C>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-115-27C>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.-6-27C>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.-6-27C>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.-6-27C>G
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10018
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3951
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8992
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 769
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1901
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5504
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3751
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1155
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 170
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21757
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5019
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2196
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1618
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2290
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
reference allele: C
site quality: DP
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-142143508-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143508
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143508
    reference: chr 4
allele count: 3
allele frequency: 2.615153945395585e-5
allele num: 114716
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.-6-12G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.-6-12G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.-6-12G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-115-12G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.-6-12G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.-6-12G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.223-12G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.-6-12G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.-6-12G>A
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28496
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1160
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 405
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4497
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10385
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 774
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1974
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1961
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5462
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 573
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 381
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1770
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1660
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: MQRankSum

4-142143510-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143510
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143510
    reference: chr 4
allele count: 1
allele frequency: 8.702159876081243e-6
allele num: 114914
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.-6-10G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.-6-10G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.-6-10G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.-6-10G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.-6-10G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.223-10G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.-6-10G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-115-10G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.-6-10G>A
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 28734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3075
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4578
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 776
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1905
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1970
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1164
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 316
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 70
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3815
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1575
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: African
reference allele: G
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD

4-142143514-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143514
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143514
    reference: chr 4
allele count: 1
allele frequency: 8.667163584045485e-6
allele num: 115378
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.-6-6A>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.-6-6A>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.-6-6A>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-115-6A>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.-6-6A>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.-6-6A>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.-6-6A>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.223-6A>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.-6-6A>T
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4512
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 574
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1990
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4726
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 28845
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1168
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 773
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1824
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11199
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2876
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 406
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1811
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 461
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1350
  bin: 3.75e1
  variant carriers: 0
hgvs: c.-6-6A>T
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
reference allele: A
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP

4-142143523-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143523
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143523
    reference: chr 4
allele count: 240
allele frequency: 2.061961956801897e-3
allele num: 116394
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-112A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.-3A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.-3A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.-3A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.-3A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.226A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.-3A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.-3A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.-3A>G
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: 5' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 551
  bin: 9.75e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 1692
  bin: 1.75e1
  variant carriers: 19
genotype depth: GenotypeDepth
  all individuals: 12393
  bin: 2.75e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3260
  bin: 1.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 2093
  bin: 3.75e1
  variant carriers: 27
genotype depth: GenotypeDepth
  all individuals: 2307
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5313
  bin: 3.25e1
  variant carriers: 46
genotype depth: GenotypeDepth
  all individuals: 28836
  bin: 2.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 38
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 793
  bin: 4.75e1
  variant carriers: 15
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 317
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.25e1
  variant carriers: 21
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3061
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1609
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1269
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 787
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 76
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD

4-142143529-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143529
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143529
    reference: chr 4
allele count: 1
allele frequency: 8.541168431841476e-6
allele num: 117080
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.4C>T
  hgvsp: ENSP00000423217.1:p.Pro2Ser
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.4C>T
  hgvsp: ENSP00000422966.1:p.Pro2Ser
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.4C>T
  hgvsp: ENSP00000427201.1:p.Pro2Ser
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.4C>T
  hgvsp: ENSP00000262990.4:p.Pro2Ser
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.4C>T
  hgvsp: ENSP00000422599.1:p.Pro2Ser
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.232C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.4C>T
  hgvsp: ENSP00000422574.1:p.Pro2Ser
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-106C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.4C>T
  hgvsp: ENSP00000422251.1:p.Pro2Ser
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 162
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 318
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1604
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 580
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1219
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 29092
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 176
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2140
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 411
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2744
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 12818
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 786
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5498
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 355
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5142
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro2Ser
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: Other
population: European (Non-Finnish)
population: South Asian
population: African
reference allele: C
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP

4-142143531-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143531
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143532
    reference: chr 4
allele count: 7
allele frequency: 6.102664248849212e-5
allele num: 114704
alternate allele: TA
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.14dupA
  hgvsp: ENSP00000262990.4:p.Thr6AspfsTer8
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.14dupA
  hgvsp: ENSP00000422966.1:p.Thr6AspfsTer8
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.14dupA
  hgvsp: ENSP00000422251.1:p.Thr6AspfsTer8
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.14dupA
  hgvsp: ENSP00000423217.1:p.Thr6AspfsTer8
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.14dupA
  hgvsp: ENSP00000427201.1:p.Thr6AspfsTer8
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.14dupA
  hgvsp: ENSP00000422599.1:p.Thr6AspfsTer8
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.14dupA
  hgvsp: ENSP00000422574.1:p.Thr6AspfsTer8
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-96dupA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.242dupA
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26493
  bin: 2.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6569
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13684
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1249
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 2.5e0
  variant carriers: 1
hgvs: p.Thr6AspfsTer8
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: Other
population: East Asian
population: South Asian
reference allele: T
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

4-142143531-TA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143531
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143530
    reference: chr 4
allele count: 9
allele frequency: 7.846282605663272e-5
allele num: 114704
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.14delA
  hgvsp: ENSP00000262990.4:p.Lys5ArgfsTer18
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.14delA
  hgvsp: ENSP00000422574.1:p.Lys5ArgfsTer18
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.242delA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.14delA
  hgvsp: ENSP00000422251.1:p.Lys5ArgfsTer18
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.14delA
  hgvsp: ENSP00000422599.1:p.Lys5ArgfsTer18
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-96delA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.14delA
  hgvsp: ENSP00000422966.1:p.Lys5ArgfsTer18
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.14delA
  hgvsp: ENSP00000423217.1:p.Lys5ArgfsTer18
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.14delA
  hgvsp: ENSP00000427201.1:p.Lys5ArgfsTer18
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 433
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13684
  bin: 2.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 885
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26493
  bin: 2.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 1725
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2543
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 183
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 642
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6569
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1958
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 232
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2460
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 308
  bin: 7.5e0
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 698
  bin: 2.5e0
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 770
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Lys5ArgfsTer18
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: TA
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff

4-142143542-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143542
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143542
    reference: chr 4
allele count: 1
allele frequency: 8.426019548365353e-6
allele num: 118680
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.17C>G
  hgvsp: ENSP00000427201.1:p.Thr6Ser
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.17C>G
  hgvsp: ENSP00000422574.1:p.Thr6Ser
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.245C>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.17C>G
  hgvsp: ENSP00000422966.1:p.Thr6Ser
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.17C>G
  hgvsp: ENSP00000422599.1:p.Thr6Ser
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.17C>G
  hgvsp: ENSP00000422251.1:p.Thr6Ser
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.17C>G
  hgvsp: ENSP00000423217.1:p.Thr6Ser
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-93C>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.17C>G
  hgvsp: ENSP00000262990.4:p.Thr6Ser
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2515
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1715
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26991
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14498
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1943
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1388
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6719
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1291
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1133
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1871
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr6Ser
num of homozygotes: 0
population: African
population: Other
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: DP

4-142143545-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143545
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143545
    reference: chr 4
allele count: 1
allele frequency: 8.413400864897609e-6
allele num: 118858
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.20G>C
  hgvsp: ENSP00000427201.1:p.Gly7Ala
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.20G>C
  hgvsp: ENSP00000422599.1:p.Gly7Ala
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.20G>C
  hgvsp: ENSP00000262990.4:p.Gly7Ala
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.20G>C
  hgvsp: ENSP00000422251.1:p.Gly7Ala
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.20G>C
  hgvsp: ENSP00000423217.1:p.Gly7Ala
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-90G>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.20G>C
  hgvsp: ENSP00000422966.1:p.Gly7Ala
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.20G>C
  hgvsp: ENSP00000422574.1:p.Gly7Ala
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.248G>C
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1825
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1210
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2523
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 128
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14638
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1708
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 22
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6785
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26977
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 845
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1391
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30930
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2223
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 762
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Gly7Ala
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: DP
site quality: QD

4-142143549-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143549
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143549
    reference: chr 4
allele count: 1
allele frequency: 8.390387971539804e-6
allele num: 119184
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.24G>A
  hgvsp: ENST00000507532.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.24G>A
  hgvsp: ENST00000503649.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.24G>A
  hgvsp: ENST00000506302.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.24G>A
  hgvsp: ENST00000262990.4:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.24G>A
  hgvsp: ENST00000512738.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-86G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.24G>A
  hgvsp: ENST00000512809.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.24G>A
  hgvsp: ENST00000515453.1:c.24G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.252G>A
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 846
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15085
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1046
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26945
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6955
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1546
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1418
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 426
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 677
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala8Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Other
reference allele: G
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD

4-142143554-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143554
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143554
    reference: chr 4
allele count: 4
allele frequency: 3.347784603538608e-5
allele num: 119482
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.257A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.29A>G
  hgvsp: ENSP00000422251.1:p.Lys10Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.29A>G
  hgvsp: ENSP00000422966.1:p.Lys10Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.29A>G
  hgvsp: ENSP00000262990.4:p.Lys10Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.29A>G
  hgvsp: ENSP00000422574.1:p.Lys10Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.29A>G
  hgvsp: ENSP00000423217.1:p.Lys10Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.29A>G
  hgvsp: ENSP00000427201.1:p.Lys10Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.29A>G
  hgvsp: ENSP00000422599.1:p.Lys10Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-81A>G
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7017
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 916
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1421
  bin: 4.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27125
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15311
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2580
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1341
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 844
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1385
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7711
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys10Arg
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
population: European (Non-Finnish)
reference allele: A
site quality: MQ
site quality: FS
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: VQSLOD

4-142143567-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143567
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143567
    reference: chr 4
allele count: 1
allele frequency: 8.341953351796856e-6
allele num: 119876
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-68C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.42C>T
  hgvsp: ENST00000503649.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.42C>T
  hgvsp: ENST00000506302.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.42C>T
  hgvsp: ENST00000512738.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.42C>T
  hgvsp: ENST00000507532.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.42C>T
  hgvsp: ENST00000512809.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.42C>T
  hgvsp: ENST00000515453.1:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.42C>T
  hgvsp: ENST00000262990.4:c.42C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.270C>T
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2623
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1012
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 722
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1429
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16689
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26290
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 603
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7331
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 6.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1114
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 471
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 456
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Asn14Asn
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: Latino
population: South Asian
population: Other
population: European (Non-Finnish)
population: African
reference allele: C
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum

4-142143569-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143569
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143569
    reference: chr 4
allele count: 1
allele frequency: 8.336112037345782e-6
allele num: 119960
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.272G>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-66G>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.44G>T
  hgvsp: ENSP00000422574.1:p.Arg15Leu
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.44G>T
  hgvsp: ENSP00000262990.4:p.Arg15Leu
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.44G>T
  hgvsp: ENSP00000422599.1:p.Arg15Leu
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.44G>T
  hgvsp: ENSP00000423217.1:p.Arg15Leu
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.44G>T
  hgvsp: ENSP00000427201.1:p.Arg15Leu
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.44G>T
  hgvsp: ENSP00000422251.1:p.Arg15Leu
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.44G>T
  hgvsp: ENSP00000422966.1:p.Arg15Leu
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 924
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 847
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 665
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7426
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2648
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16891
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 608
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26221
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 850
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1441
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 375
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 270
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Arg15Leu
num of homozygotes: 0
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: VQSLOD

4-142143572-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143572
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143572
    reference: chr 4
allele count: 1
allele frequency: 8.31766839119658e-6
allele num: 120226
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.47G>A
  hgvsp: ENSP00000427201.1:p.Arg16Gln
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.47G>A
  hgvsp: ENSP00000422599.1:p.Arg16Gln
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.47G>A
  hgvsp: ENSP00000262990.4:p.Arg16Gln
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.47G>A
  hgvsp: ENSP00000422966.1:p.Arg16Gln
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.47G>A
  hgvsp: ENSP00000422574.1:p.Arg16Gln
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.47G>A
  hgvsp: ENSP00000422251.1:p.Arg16Gln
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.47G>A
  hgvsp: ENSP00000423217.1:p.Arg16Gln
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-63G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.275G>A
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17137
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 756
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2664
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 228
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26328
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7494
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 322
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 556
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 607
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 678
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 545
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 390
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2322
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Arg16Gln
num of homozygotes: 0
population: European (Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
reference allele: G
site quality: QD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: DP

4-142143573-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143573
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143573
    reference: chr 4
allele count: 3
allele frequency: 2.49260527102928e-5
allele num: 120356
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.48A>G
  hgvsp: ENST00000506302.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.276A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.48A>G
  hgvsp: ENST00000512738.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-62A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.48A>G
  hgvsp: ENST00000262990.4:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.48A>G
  hgvsp: ENST00000507532.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.48A>G
  hgvsp: ENST00000503649.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.48A>G
  hgvsp: ENST00000512809.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.48A>G
  hgvsp: ENST00000515453.1:c.48A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 519
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 413
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7486
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 851
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 719
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2662
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 629
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26417
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1452
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1175
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg16Arg
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: A
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum

4-142143597-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143597
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143597
    reference: chr 4
allele count: 1
allele frequency: 8.267605866693123e-6
allele num: 120954
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.72A>G
  hgvsp: ENST00000262990.4:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.72A>G
  hgvsp: ENST00000506302.1:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.72A>G
  hgvsp: ENST00000507532.1:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.300A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.72A>G
  hgvsp: ENST00000503649.1:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.72A>G
  hgvsp: ENST00000512738.1:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.72A>G
  hgvsp: ENST00000515453.1:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-38A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.72A>G
  hgvsp: ENST00000512809.1:c.72A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 852
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7601
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2675
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 546
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17608
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27024
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 220
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8164
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ala24Ala
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: ClippingRankSum
site quality: DP
site quality: QD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-142143600-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143600
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143600
    reference: chr 4
allele count: 1
allele frequency: 8.26405302216419e-6
allele num: 121006
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-35A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.75A>C
  hgvsp: ENST00000506302.1:c.75A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.75A>C
  hgvsp: ENST00000503649.1:c.75A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.75A>C
  hgvsp: ENST00000512809.1:c.75A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.75A>C
  hgvsp: ENST00000507532.1:c.75A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.303A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.75A>C
  hgvsp: ENST00000515453.1:c.75A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.75A>C
  hgvsp: ENST00000512738.1:c.75A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.75A>C
  hgvsp: ENST00000262990.4:c.75A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 191
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 414
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7613
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 113
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 606
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17634
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2678
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 246
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27077
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 853
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 165
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 127
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 547
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 328
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Ser25Ser
num of homozygotes: 0
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD

4-142143607-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143607
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143607
    reference: chr 4
allele count: 687
allele frequency: 5.67374715073833e-3
allele num: 121084
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.82A>G
  hgvsp: ENSP00000427201.1:p.Thr28Ala
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.82A>G
  hgvsp: ENSP00000262990.4:p.Thr28Ala
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-28A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.310A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.82A>G
  hgvsp: ENSP00000422599.1:p.Thr28Ala
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.82A>G
  hgvsp: ENSP00000422251.1:p.Thr28Ala
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.82A>G
  hgvsp: ENSP00000423217.1:p.Thr28Ala
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.82A>G
  hgvsp: ENSP00000422574.1:p.Thr28Ala
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.82A>G
  hgvsp: ENSP00000422966.1:p.Thr28Ala
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 159
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 8.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 7.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 677
  bin: 5.25e1
  variant carriers: 78
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 468
  bin: 5.75e1
  variant carriers: 61
genotype depth: GenotypeDepth
  all individuals: 371
  bin: 6.25e1
  variant carriers: 58
genotype depth: GenotypeDepth
  all individuals: 937
  bin: 4.75e1
  variant carriers: 89
genotype depth: GenotypeDepth
  all individuals: 143
  bin: 8.25e1
  variant carriers: 16
genotype depth: GenotypeDepth
  all individuals: 7566
  bin: 3.25e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 9.25e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 198
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 264
  bin: 6.75e1
  variant carriers: 39
genotype depth: GenotypeDepth
  all individuals: 26842
  bin: 2.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 2682
  bin: 3.75e1
  variant carriers: 38
genotype depth: GenotypeDepth
  all individuals: 208
  bin: 7.25e1
  variant carriers: 32
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 9.75e1
  variant carriers: 91
genotype depth: GenotypeDepth
  all individuals: 17508
  bin: 2.75e1
  variant carriers: 17
genotype depth: GenotypeDepth
  all individuals: 1502
  bin: 4.25e1
  variant carriers: 63
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr28Ala
num of homozygotes: 5
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
population: Latino
reference allele: A
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: QD

4-142143611-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143611
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143611
    reference: chr 4
allele count: 1
allele frequency: 8.257911078813503e-6
allele num: 121096
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.86T>G
  hgvsp: ENSP00000422599.1:p.Ile29Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.314T>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.86T>G
  hgvsp: ENSP00000423217.1:p.Ile29Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.86T>G
  hgvsp: ENSP00000427201.1:p.Ile29Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.86T>G
  hgvsp: ENSP00000422251.1:p.Ile29Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.86T>G
  hgvsp: ENSP00000422966.1:p.Ile29Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-24T>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.86T>G
  hgvsp: ENSP00000422574.1:p.Ile29Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.86T>G
  hgvsp: ENSP00000262990.4:p.Ile29Arg
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26868
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7690
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 17733
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5389
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 3622
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile29Arg
num of homozygotes: 0
population: African
population: Other
population: South Asian
population: East Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

4-142143613-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143613
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143613
    reference: chr 4
allele count: 1
allele frequency: 8.257638315441784e-6
allele num: 121100
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.88G>A
  hgvsp: ENSP00000422966.1:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.88G>A
  hgvsp: ENSP00000427201.1:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.316G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.88G>A
  hgvsp: ENSP00000422574.1:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.88G>A
  hgvsp: ENSP00000422251.1:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.88G>A
  hgvsp: ENSP00000262990.4:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.88G>A
  hgvsp: ENSP00000422599.1:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.88G>A
  hgvsp: ENSP00000423217.1:p.Asp30Asn
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-22G>A
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Asp30Asn
num of homozygotes: 0
population: East Asian
population: South Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: QD

4-142143613-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143613
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143613
    reference: chr 4
allele count: 1
allele frequency: 8.257638315441784e-6
allele num: 121100
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.88G>C
  hgvsp: ENSP00000422599.1:p.Asp30His
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.88G>C
  hgvsp: ENSP00000423217.1:p.Asp30His
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.88G>C
  hgvsp: ENSP00000422966.1:p.Asp30His
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.88G>C
  hgvsp: ENSP00000427201.1:p.Asp30His
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.316G>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.88G>C
  hgvsp: ENSP00000422251.1:p.Asp30His
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.88G>C
  hgvsp: ENSP00000422574.1:p.Asp30His
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-22G>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.88G>C
  hgvsp: ENSP00000262990.4:p.Asp30His
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 184
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1508
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 883
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26874
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7691
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17751
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 117
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3620
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Asp30His
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Other
population: Latino
reference allele: G
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD

4-142143632-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143632
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143632
    reference: chr 4
allele count: 1
allele frequency: 8.25559316436886e-6
allele num: 121130
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.107G>A
  hgvsp: ENSP00000422251.1:p.Cys36Tyr
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.107G>A
  hgvsp: ENSP00000422966.1:p.Cys36Tyr
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_donor_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.106+1G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.335G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.107G>A
  hgvsp: ENSP00000422599.1:p.Cys36Tyr
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.107G>A
  hgvsp: ENSP00000262990.4:p.Cys36Tyr
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.107G>A
  hgvsp: ENSP00000423217.1:p.Cys36Tyr
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 5_prime_UTR_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.-3G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.107G>A
  hgvsp: ENSP00000427201.1:p.Cys36Tyr
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: splice donor
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 26864
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2720
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 425
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7695
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17813
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5389
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 8223
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3609
  bin: 7.75e1
  variant carriers: 0
hgvs: c.106+1G>A
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
population: African
reference allele: G
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: FS
site quality: QD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

4-142143641-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143641
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143641
    reference: chr 4
allele count: 1
allele frequency: 8.259820927082301e-6
allele num: 121068
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.116C>T
  hgvsp: ENSP00000422599.1:p.Ser39Leu
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.116C>T
  hgvsp: ENSP00000422966.1:p.Ser39Leu
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.7C>T
  hgvsp: ENSP00000397397.2:p.Gln3Ter
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.116C>T
  hgvsp: ENSP00000427201.1:p.Ser39Leu
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.116C>T
  hgvsp: ENSP00000262990.4:p.Ser39Leu
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.116C>T
  hgvsp: ENSP00000422251.1:p.Ser39Leu
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.344C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.116C>T
  hgvsp: ENSP00000423217.1:p.Ser39Leu
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.106+10C>T
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7698
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26574
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 333
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17843
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 149
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 918
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35055
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Gln3Ter
num of homozygotes: 0
population: African
population: Other
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD

4-142143643-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143643
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143643
    reference: chr 4
allele count: 2
allele frequency: 1.652073352056831e-5
allele num: 121060
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.106+12A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.346A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.118A>G
  hgvsp: ENSP00000262990.4:p.Met40Val
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.118A>G
  hgvsp: ENSP00000423217.1:p.Met40Val
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.118A>G
  hgvsp: ENSP00000427201.1:p.Met40Val
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.118A>G
  hgvsp: ENSP00000422251.1:p.Met40Val
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.118A>G
  hgvsp: ENSP00000422966.1:p.Met40Val
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.118A>G
  hgvsp: ENSP00000422599.1:p.Met40Val
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.9A>G
  hgvsp: ENST00000421169.2:c.9A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 880
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 625
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26553
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 160
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7694
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17842
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2718
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 346
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 171
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 8.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 64
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 117
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Met40Val
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: European (Finnish)
population: Other
population: Latino
population: African
population: South Asian
reference allele: A
site quality: MQ
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

4-142143651-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143651
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143651
    reference: chr 4
allele count: 1
allele frequency: 8.265009256810368e-6
allele num: 120992
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.120+6A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.106+20A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.120+6A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.120+6A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.120+6A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.11+6A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.120+6A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.354A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.120+6A>G
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 624
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 882
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7686
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17720
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 479
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2722
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1510
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26435
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8195
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34770
  bin: 6.25e1
  variant carriers: 0
hgvs: c.120+6A>G
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD

4-142143653-CT-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143653
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143652
    reference: chr 4
allele count: 2
allele frequency: 1.654807214959457e-5
allele num: 120860
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.120+15delT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.120+15delT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.106+29delT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.11+15delT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.120+15delT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.120+15delT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.363delT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.120+15delT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.120+15delT
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: non coding transcript exon
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 26198
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2756
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 899
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 515
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17702
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 323
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7786
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1538
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 427
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 632
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 258
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 140
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34441
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8103
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 108
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 206
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
reference allele: CT
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQ

4-142143662-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143662
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143662
    reference: chr 4
allele count: 2
allele frequency: 1.654095540558423e-5
allele num: 120912
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.365A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.120+17A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.120+17A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.120+17A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.120+17A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.120+17A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.106+31A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.120+17A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.11+17A>G
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 240
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 623
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1506
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 10
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17758
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 446
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25763
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7674
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2343
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 193
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQ
site quality: BaseQRankSum

4-142143668-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143668
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143668
    reference: chr 4
allele count: 1
allele frequency: 8.276227364518158e-6
allele num: 120828
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.120+23G>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.120+23G>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.11+23G>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.120+23G>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.120+23G>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.106+37G>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.371G>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.120+23G>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.120+23G>C
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2724
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1068
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1507
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1412
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7646
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17425
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24937
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1005
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1203
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 459
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3087
  bin: 7.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: East Asian
population: African
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: MQ
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum

4-142143669-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143669
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143669
    reference: chr 4
allele count: 2
allele frequency: 1.655245472903632e-5
allele num: 120828
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.120+24T>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.106+38T>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.11+24T>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.120+24T>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.372T>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.120+24T>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.120+24T>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.120+24T>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.120+24T>G
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17427
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24947
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 181
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7634
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 544
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 879
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1509
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 267
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2723
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1065
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 234
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1413
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 418
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 197
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum

4-142143686-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143686
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143686
    reference: chr 4
allele count: 1
allele frequency: 8.290361625574107e-6
allele num: 120622
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.120+41T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.120+41T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.389T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.106+55T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.120+41T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.120+41T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.120+41T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.11+41T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.120+41T>C
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 877
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1887
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2687
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15594
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4382
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23258
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1501
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7329
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 424
  bin: 5.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 832
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 219
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 801
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1342
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: Latino
population: South Asian
population: African
reference allele: T
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: MQ

4-142143687-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143687
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143687
    reference: chr 4
allele count: 1
allele frequency: 8.290224167661493e-6
allele num: 120624
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.390A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.120+42A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.120+42A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.106+56A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.120+42A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.11+42A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.120+42A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.120+42A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.120+42A>G
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15607
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23256
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1892
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7328
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4376
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 331
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2683
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1496
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1032
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1199
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1714
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1347
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: East Asian
population: European (Finnish)
population: African
reference allele: A
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: QD

4-142143689-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143689
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143689
    reference: chr 4
allele count: 1
allele frequency: 8.297240337863626e-6
allele num: 120522
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.120+44A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.120+44A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.106+58A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.120+44A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.11+44A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.392A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.120+44A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.120+44A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.120+44A>G
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1872
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14930
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 621
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2673
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 367
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4365
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24039
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 26184
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1307
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 914
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: QD

4-142143694-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143694
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143694
    reference: chr 4
allele count: 1
allele frequency: 8.309788931361144e-6
allele num: 120340
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.11+49A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.120+49A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.397A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.120+49A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.120+49A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.120+49A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.120+49A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.120+49A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.106+63A>G
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24129
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4326
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14959
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1491
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1866
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2663
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5390
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 167
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2996
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 916
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: Other
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP

4-142143695-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142143695
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142143695
    reference: chr 4
allele count: 1
allele frequency: 8.311999202048076e-6
allele num: 120308
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.120+50T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.120+50T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.120+50T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000109445
  ensembl transcript: ENST00000514826
  gene symbol: ZNF330
  hgvsc: ENST00000514826.1:n.398T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.120+50T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.11+50T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.106+64T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.120+50T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.120+50T>C
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: non coding transcript exon
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4322
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 321
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 167
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 423
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1492
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 33
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24090
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 235
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7115
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1869
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 415
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 878
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 543
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2665
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 622
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14998
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3482
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2995
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2474
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 338
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5390
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: African
population: European (Finnish)
population: East Asian
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: QD

4-142144905-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142144905
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142144905
    reference: chr 4
allele count: 1
allele frequency: 9.316191540898081e-5
allele num: 10734
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12-736G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121-736G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121-736G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121-736G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107-736G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121-736G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121-736G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.121-18G>A
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1230
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 724
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1954
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 961
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1081
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1622
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 500
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 323
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 814
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 9.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD

4-142144909-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142144909
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142144909
    reference: chr 4
allele count: 1
allele frequency: 9.316191540898081e-5
allele num: 10734
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121-732A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.121-14A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121-732A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121-732A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121-732A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107-732A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12-732A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121-732A>G
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1082
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 969
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1955
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 319
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 435
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1954
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 817
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: DP

4-142144917-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142144917
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142144917
    reference: chr 4
allele count: 1
allele frequency: 9.312721177127957e-5
allele num: 10738
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107-724T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121-724T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121-724T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121-724T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12-724T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121-724T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121-724T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.121-6T>C
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1917
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 660
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 395
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 972
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1226
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1636
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 278
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.75e1
  variant carriers: 0
hgvs: c.121-6T>C
num of homozygotes: 0
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: Other
reference allele: T
site quality: BaseQRankSum
site quality: MQ
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

4-142144920-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142144920
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142144920
    reference: chr 4
allele count: 1
allele frequency: 9.310986964618249e-5
allele num: 10740
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107-721T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121-721T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.121-3T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121-721T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121-721T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12-721T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121-721T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121-721T>C
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 72
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1084
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1228
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1920
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 177
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 657
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 725
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 973
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 303
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1653
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1954
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 482
  bin: 6.75e1
  variant carriers: 0
hgvs: c.121-3T>C
num of homozygotes: 0
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: Other
population: European (Finnish)
reference allele: T
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

4-142144966-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142144966
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142144966
    reference: chr 4
allele count: 1
allele frequency: 9.305788200260562e-5
allele num: 10746
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107-675T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12-675T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121-675T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000423217
  ensembl transcript: ENST00000515453
  gene symbol: ZNF330
  hgvsc: ENST00000515453.1:c.*38T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121-675T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121-675T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121-675T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121-675T>C
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: 3' UTR
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 577
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 394
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 989
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2241
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 178
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1085
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 726
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1237
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 34
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 507
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 470
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1731
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: T
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum

4-142145590-TG-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145590
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145589
    reference: chr 4
allele count: 2
allele frequency: 1.659668398254029e-5
allele num: 120506
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121-50delG
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121-50delG
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121-50delG
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121-50delG
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107-50delG
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12-50delG
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121-50delG
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1346
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4184
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 704
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2245
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4811
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 155
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 238
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 326
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2405
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1436
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2592
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 541
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1579
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: South Asian
population: Latino
population: African
population: Other
reference allele: TG
site quality: VQSLOD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD

4-142145594-GT-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145594
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145593
    reference: chr 4
allele count: 1
allele frequency: 8.297240337863626e-6
allele num: 120522
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121-43delT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121-43delT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12-43delT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121-43delT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121-43delT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107-43delT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121-43delT
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 697
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4818
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 980
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1043
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4222
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2512
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 301
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5598
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2562
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 138
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1439
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 313
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 346
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4685
  bin: 6.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: European (Non-Finnish)
population: Other
reference allele: GT
site quality: VQSLOD
site quality: FS
site quality: MQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: DP
site quality: MQ

4-142145603-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145603
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145603
    reference: chr 4
allele count: 1
allele frequency: 8.297653423611802e-6
allele num: 120516
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121-38C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121-38C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121-38C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107-38C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12-38C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121-38C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121-38C>T
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 303
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4880
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3074
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4359
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 558
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 422
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5600
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 349
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2886
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2569
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 221
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5433
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 91
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
reference allele: C
site quality: ReadPosRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP

4-142145608-GA-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145608
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145607
    reference: chr 4
allele count: 1
allele frequency: 8.2936619835122e-6
allele num: 120574
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12-28delA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121-28delA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121-28delA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121-28delA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107-28delA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121-28delA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121-28delA
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 295
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4459
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 202
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3344
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6301
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 388
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4903
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 149
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 162
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40138
  bin: 9.75e1
  variant carriers: 1
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
reference allele: GA
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/4-142145609-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145609
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145609
    reference: chr 4
allele count: 1
allele frequency: 8.29324929507381e-6
allele num: 120580
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121-32A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121-32A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121-32A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12-32A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121-32A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107-32A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121-32A>C
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4898
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 365
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4465
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6697
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 292
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3396
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 333
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 139
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2711
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2890
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2411
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: Other
population: Latino
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQ
site quality: QD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: DP

http://identifiers.org/exac.variant/4-142145611-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145611
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145611
    reference: chr 4
allele count: 1
allele frequency: 8.292148993333113e-6
allele num: 120596
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121-30A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121-30A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121-30A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121-30A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12-30A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121-30A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107-30A>C
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2765
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4896
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4480
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3478
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5606
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 319
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2582
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2412
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 126
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 324
  bin: 2.25e1
  variant carriers: 0
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: Latino
population: Other
population: South Asian
population: European (Finnish)
population: African
reference allele: A
site quality: QD
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: MQRankSum
site quality: VQSLOD

4-142145618-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145618
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145618
    reference: chr 4
allele count: 13
allele frequency: 1.07731830612414e-4
allele num: 120670
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12-23T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121-23T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107-23T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121-23T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121-23T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121-23T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121-23T>C
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4905
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3663
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4522
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 979
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4071
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6893
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3786
  bin: 9.75e1
  variant carriers: 5
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 50
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2583
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2412
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1461
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 296
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  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2733
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
population: African
population: European (Finnish)
reference allele: T
site quality: VQSLOD
site quality: DP
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-142145628-T-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145628
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145628
    reference: chr 4
allele count: 1
allele frequency: 8.283906027370025e-6
allele num: 120716
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121-13T>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121-13T>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121-13T>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121-13T>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12-13T>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121-13T>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107-13T>A
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4910
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4568
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5605
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 40
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3708
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2891
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1462
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1585
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 269
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2583
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 83
  bin: 7.5e0
  variant carriers: 0
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: European (Non-Finnish)
population: East Asian
reference allele: T
site quality: DP
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: QD

4-142145636-T-TA
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145636
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145637
    reference: chr 4
allele count: 1
allele frequency: 8.282533792737874e-6
allele num: 120736
alternate allele: TA
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107-4dupA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121-4dupA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121-4dupA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121-4dupA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12-4dupA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121-4dupA
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121-4dupA
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: splice region
filter: VQSRTrancheINDEL99.00to99.50
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3713
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4070
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1914
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5604
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 129
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4908
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6897
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1459
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2891
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 267
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
hgvs: c.121-4dupA
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: African
population: South Asian
population: East Asian
population: European (Finnish)
population: Other
reference allele: T
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: QD
site quality: VQSLOD
site quality: DP
site quality: MQ

4-142145641-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145641
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145641
    reference: chr 4
allele count: 3
allele frequency: 2.484595507851322e-5
allele num: 120744
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.121G>A
  hgvsp: ENSP00000422251.1:p.Glu41Lys
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.121G>A
  hgvsp: ENSP00000427201.1:p.Glu41Lys
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: stop_gained
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.12G>A
  hgvsp: ENSP00000397397.2:p.Trp4Ter
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.121G>A
  hgvsp: ENSP00000422599.1:p.Glu41Lys
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.121G>A
  hgvsp: ENSP00000422966.1:p.Glu41Lys
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.121G>A
  hgvsp: ENSP00000262990.4:p.Glu41Lys
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: stop_retained_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.107G>A
  hgvsp: ENST00000507532.1:c.107G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
canonical: false
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5305
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 219
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5605
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6696
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3702
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 56
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 8.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 126
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4912
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2751
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2891
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Trp4Ter
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
population: Other
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: DP

4-142145666-TTTTA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145666
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145662
    reference: chr 4
allele count: 1
allele frequency: 8.286651861182008e-6
allele num: 120676
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.140+10_140+13delATTT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*18+10_*18+13delATTT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+10_31+13delATTT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.140+10_140+13delATTT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.140+10_140+13delATTT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.140+10_140+13delATTT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+10_140+13delATTT
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 180
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 214
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4892
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6694
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 146
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 190
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3549
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5599
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4509
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 40129
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2575
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 148
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2892
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2717
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 65
  bin: 4.75e1
  variant carriers: 0
hgvs: c.140+10_140+13delATTT
num of homozygotes: 0
population: Other
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: TTTTA
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: QD
site quality: InbreedingCoeff

4-142145674-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145674
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145674
    reference: chr 4
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*18+14C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.140+14C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.140+14C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.140+14C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.140+14C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+14C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+14C>T
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5601
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 272
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 201
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6897
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 156
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4873
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4463
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3778
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2389
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 93
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40126
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1581
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2892
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2690
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: East Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
reference allele: C
site quality: VQSLOD
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS

4-142145679-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145679
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145679
    reference: chr 4
allele count: 2
allele frequency: 1.657907389293234e-5
allele num: 120634
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.140+19T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.140+19T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+19T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.140+19T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*18+19T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.140+19T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+19T>C
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4860
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3534
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5598
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 173
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6694
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6300
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4462
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 279
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2578
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2893
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1447
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 103
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: Latino
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum

4-142145680-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145680
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145680
    reference: chr 4
allele count: 1
allele frequency: 8.289674381590291e-6
allele num: 120632
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*18+20C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+20C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.140+20C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.140+20C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+20C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.140+20C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.140+20C>T
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4864
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2768
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1362
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 275
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6298
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 172
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 155
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4464
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3776
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5307
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2893
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1581
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2578
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 78
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 86
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 107
  bin: 3.25e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Latino
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: East Asian
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: QD

http://identifiers.org/exac.variant/4-142145686-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145686
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145686
    reference: chr 4
allele count: 2
allele frequency: 1.658044833532299e-5
allele num: 120624
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.140+26A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*18+26A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.140+26A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+26A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+26A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.140+26A>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.140+26A>C
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 231
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6695
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6299
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4831
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 174
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5306
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 304
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3544
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2769
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1361
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 87
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 77
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 120
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 235
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40126
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 5957
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1437
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 166
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2384
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: Other
population: European (Finnish)
population: Latino
population: African
population: East Asian
population: European (Non-Finnish)
reference allele: A
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ReadPosRankSum

4-142145706-TCTGA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145706
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145702
    reference: chr 4
allele count: 2
allele frequency: 1.658209796703479e-5
allele num: 120612
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.141-49_140+49delGACT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.141-49_140+49delGACT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+49_31+52delGACT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.141-49_140+49delGACT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+49_140+52delGACT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.141-49_140+49delGACT
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*18+49_*19-49delGACT
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 164
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 375
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 194
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4068
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 239
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3654
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4755
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 593
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6893
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 80
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2390
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1433
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 275
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40118
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2628
  bin: 6.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: Other
reference allele: TCTGA
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: QD
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-142145716-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145716
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145716
    reference: chr 4
allele count: 1
allele frequency: 8.289949265510494e-6
allele num: 120628
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+56T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.141-45T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+56T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.141-45T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.141-45T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*19-45T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.141-45T>C
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 199
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4751
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 337
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5574
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2767
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3732
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 236
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4336
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 129
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5927
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 111
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2577
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 160
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1429
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2387
  bin: 7.75e1
  variant carriers: 0
num of homozygotes: 0
population: African
population: Other
population: European (Finnish)
population: Latino
population: East Asian
population: European (Non-Finnish)
population: South Asian
reference allele: T
site quality: DP
site quality: FS
site quality: QD
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum

4-142145717-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145717
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145717
    reference: chr 4
allele count: 1
allele frequency: 8.288987251537607e-6
allele num: 120642
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*19-44A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.141-44A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+57A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+57A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.141-44A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.141-44A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.141-44A>G
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4344
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5576
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 154
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6679
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 324
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4752
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3734
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 164
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 102
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 280
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 88
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5970
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2889
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1430
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 79
  bin: 5.25e1
  variant carriers: 0
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: Other
reference allele: A
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: DP

4-142145723-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145723
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145723
    reference: chr 4
allele count: 1
allele frequency: 8.289399515899069e-6
allele num: 120636
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+63C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*19-38C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.141-38C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.141-38C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+63C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.141-38C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.141-38C>T
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6297
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4767
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5578
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5308
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 221
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1912
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4373
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6891
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 134
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6686
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3737
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1360
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 592
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 288
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3777
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 85
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1423
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 98
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 307
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2391
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 112
  bin: 3.75e1
  variant carriers: 0
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: East Asian
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: QD

4-142145732-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145732
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145732
    reference: chr 4
allele count: 121
allele frequency: 1.002585178311017e-3
allele num: 120688
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+72T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+72T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.141-29T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.141-29T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*19-29T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.141-29T>C
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.141-29T>C
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: intron
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 734
  bin: 8.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 3781
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4417
  bin: 2.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6891
  bin: 4.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 226
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2766
  bin: 6.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 6680
  bin: 4.25e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 211
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3782
  bin: 9.75e1
  variant carriers: 11
genotype depth: GenotypeDepth
  all individuals: 983
  bin: 8.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 4077
  bin: 6.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1913
  bin: 7.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 1363
  bin: 7.75e1
  variant carriers: 10
genotype depth: GenotypeDepth
  all individuals: 4759
  bin: 3.25e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 212
  bin: 1.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5575
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5320
  bin: 5.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 596
  bin: 9.25e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 6296
  bin: 5.25e1
  variant carriers: 14
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 297
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6166
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1419
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1576
  bin: 8.75e1
  variant carriers: 0
num of homozygotes: 5
population: South Asian
population: Latino
population: African
population: Other
population: European (Finnish)
population: East Asian
population: European (Non-Finnish)
reference allele: T
site quality: ClippingRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

4-142145753-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145753
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145753
    reference: chr 4
allele count: 1
allele frequency: 8.271161767381846e-6
allele num: 120902
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.141-8A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*19-8A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.141-8A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+93A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.141-8A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.141-8A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+93A>G
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: splice region
filter: VQSRTrancheSNP99.60to99.80
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4807
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 114
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 227
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6894
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4514
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1428
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2665
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2395
  bin: 7.75e1
  variant carriers: 0
hgvs: c.141-8A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: South Asian
population: Latino
population: Other
population: East Asian
population: African
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum

4-142145757-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145757
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145757
    reference: chr 4
allele count: 1
allele frequency: 8.266512358435975e-6
allele num: 120970
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*19-4C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+97C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.141-4C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.141-4C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.141-4C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.141-4C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+97C>T
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6896
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6693
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4063
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 50
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5590
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 95
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4536
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 196
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4801
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40113
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1426
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2580
  bin: 8.25e1
  variant carriers: 0
hgvs: c.141-4C>T
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
population: European (Finnish)
population: East Asian
population: Latino
reference allele: C
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP

4-142145758-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145758
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145758
    reference: chr 4
allele count: 1
allele frequency: 8.264872638312644e-6
allele num: 120994
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.141-3A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+98A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*19-3A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.141-3A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+98A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.141-3A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: splice_region_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.141-3A>G
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4548
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4066
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1909
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 187
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5589
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6895
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 52
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6692
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2894
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.25e1
  variant carriers: 0
hgvs: c.141-3A>G
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: South Asian
population: African
population: Other
population: East Asian
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: BaseQRankSum

http://identifiers.org/exac.variant/4-142145762-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145762
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145762
    reference: chr 4
allele count: 2
allele frequency: 1.652237129072764e-5
allele num: 121048
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.142C>A
  hgvsp: ENST00000503649.1:c.142C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.142C>A
  hgvsp: ENST00000512738.1:c.142C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+102C>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*20C>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+102C>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.142C>A
  hgvsp: ENST00000262990.4:c.142C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.142C>A
  hgvsp: ENST00000512809.1:c.142C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: splice region
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 3.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6687
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2672
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40113
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
hgvs: c.142C>A
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: European (Finnish)
population: Other
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: DP
site quality: ReadPosRankSum
site quality: QD

4-142145762-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145762
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145762
    reference: chr 4
allele count: 4
allele frequency: 3.304474258145529e-5
allele num: 121048
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+102C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.142C>T
  hgvsp: ENSP00000422966.1:p.Arg48Trp
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.142C>T
  hgvsp: ENSP00000422599.1:p.Arg48Trp
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+102C>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.142C>T
  hgvsp: ENSP00000422251.1:p.Arg48Trp
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.142C>T
  hgvsp: ENSP00000262990.4:p.Arg48Trp
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*20C>T
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 47
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4804
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 163
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1353
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5316
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5596
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2761
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4560
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4093
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 590
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3775
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6892
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 198
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2894
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg48Trp
num of homozygotes: 0
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
population: African
population: Latino
population: East Asian
reference allele: C
site quality: FS
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

4-142145763-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145763
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145763
    reference: chr 4
allele count: 4
allele frequency: 3.30376463980706e-5
allele num: 121074
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+103G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+103G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.143G>A
  hgvsp: ENSP00000422966.1:p.Arg48Gln
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.143G>A
  hgvsp: ENSP00000422251.1:p.Arg48Gln
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: splice_region_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*21G>A
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.143G>A
  hgvsp: ENSP00000422599.1:p.Arg48Gln
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  consequence: splice_region_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.143G>A
  hgvsp: ENSP00000262990.4:p.Arg48Gln
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 591
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3774
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 46
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6293
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5592
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4103
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 727
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2759
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1354
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 76
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4803
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 157
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4069
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6892
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6691
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 976
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1911
  bin: 7.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2581
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Arg48Gln
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Non-Finnish)
population: African
population: Other
population: Latino
population: European (Finnish)
reference allele: G
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: QD
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: ReadPosRankSum

4-142145769-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145769
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145769
    reference: chr 4
allele count: 22
allele frequency: 1.816380449141347e-4
allele num: 121120
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.149A>G
  hgvsp: ENSP00000422251.1:p.Lys50Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.149A>G
  hgvsp: ENSP00000262990.4:p.Lys50Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.149A>G
  hgvsp: ENSP00000422599.1:p.Lys50Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+109A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.149A>G
  hgvsp: ENSP00000422966.1:p.Lys50Arg
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*27A>G
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+109A>G
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6690
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4583
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1359
  bin: 7.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3779
  bin: 9.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 975
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4138
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4798
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5586
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2763
  bin: 6.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 37
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 8.75e1
  variant carriers: 5
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6288
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6890
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5318
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4066
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2677
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Lys50Arg
num of homozygotes: 1
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

4-142145770-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 142145770
    reference: chr 4
  end: Position
    type: ExactPosition
    position: 142145770
    reference: chr 4
allele count: 1
allele frequency: 8.256002113536541e-6
allele num: 121124
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000262990
  ensembl transcript: ENST00000262990
  gene symbol: ZNF330
  hgvsc: ENST00000262990.4:c.150G>T
  hgvsp: ENSP00000262990.4:p.Lys50Asn
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000427201
  ensembl transcript: ENST00000506302
  gene symbol: ZNF330
  hgvsc: ENST00000506302.1:c.140+110G>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: 3_prime_UTR_variant
  consequence: NMD_transcript_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422574
  ensembl transcript: ENST00000507532
  gene symbol: ZNF330
  hgvsc: ENST00000507532.1:c.*28G>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422251
  ensembl transcript: ENST00000512738
  gene symbol: ZNF330
  hgvsc: ENST00000512738.1:c.150G>T
  hgvsp: ENSP00000422251.1:p.Lys50Asn
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422599
  ensembl transcript: ENST00000512809
  gene symbol: ZNF330
  hgvsc: ENST00000512809.1:c.150G>T
  hgvsp: ENSP00000422599.1:p.Lys50Asn
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000397397
  ensembl transcript: ENST00000421169
  gene symbol: ZNF330
  hgvsc: ENST00000421169.2:c.31+110G>T
  variant of: http://identifiers.org/hgnc/15462
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000109445
  ensembl protein: ENSP00000422966
  ensembl transcript: ENST00000503649
  gene symbol: ZNF330
  hgvsc: ENST00000503649.1:c.150G>T
  hgvsp: ENSP00000422966.1:p.Lys50Asn
  variant of: http://identifiers.org/hgnc/15462
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 59
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 977
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2760
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 589
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4582
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6292
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1356
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6891
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5317
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1910
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4146
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Lys50Asn
num of homozygotes: 0
reference allele: G

GenotypeQuality
all individuals: 5034
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 3977
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 14521
bin: 6.25e1
variant carriers: 0

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 frequency: 2.012801417012198e-5
allele num: 49682
num of homozygotes: 0

Other
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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South Asian
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East Asian
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allele frequency: 0.0e0
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African
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BaseQRankSum
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VQSLOD
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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MQ
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QD
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

Latino
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num of homozygotes: 0

European (Non-Finnish)
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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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num of homozygotes: 0

African
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allele frequency: 1.045587620242576e-4
allele num: 9564
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 frequency: 0.0e0
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Other
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QD
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FS
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MQRankSum
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VQSLOD
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ClippingRankSum
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DP
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ReadPosRankSum
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MQ
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InbreedingCoeff
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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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variant carriers: 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 frequency: 0.0e0
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num of homozygotes: 0

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

Latino
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allele frequency: 9.139097057210747e-5
allele num: 10942
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9566
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 61784
num of homozygotes: 0

ReadPosRankSum
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SIO_000300: 1.62e0

BaseQRankSum
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DP
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MQ
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ClippingRankSum
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FS
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MQRankSum
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QD
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InbreedingCoeff
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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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Latino
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allele frequency: 0.0e0
allele num: 10982
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
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South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15174
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European (Non-Finnish)
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allele count: 3
allele frequency: 4.838241460503822e-5
allele num: 62006
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 1.446524e6

FS
type: SiteQuality
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QD
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ReadPosRankSum
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MQRankSum
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VQSLOD
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MQ
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ClippingRankSum
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InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 7.08e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 3

GenotypeQuality
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variant carriers: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9762
num of homozygotes: 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: 4.771144120360062e-5
allele num: 62878
num of homozygotes: 0

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

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 15450
num of homozygotes: 0

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

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

VQSLOD
type: SiteQuality
SIO_000300: 1.25e0

ClippingRankSum
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DP
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.261e0

BaseQRankSum
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SIO_000300: -1.763e0

MQ
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.194e1

MQRankSum
type: SiteQuality
SIO_000300: 2.89e-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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Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11098
num of homozygotes: 0

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

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

European (Non-Finnish)
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allele frequency: 1.586495748191395e-5
allele num: 63032
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South Asian
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East Asian
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allele frequency: 0.0e0
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African
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VQSLOD
type: SiteQuality
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ClippingRankSum
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BaseQRankSum
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MQ
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FS
type: SiteQuality
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DP
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ReadPosRankSum
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InbreedingCoeff
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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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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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
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African
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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

European (Non-Finnish)
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allele frequency: 1.580078371887246e-5
allele num: 63288
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ClippingRankSum
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BaseQRankSum
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FS
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QD
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InbreedingCoeff
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VQSLOD
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MQ
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ReadPosRankSum
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MQRankSum
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele count: 184
allele frequency: 2.878958568031043e-3
allele num: 63912
num of homozygotes: 0

South Asian
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East Asian
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European (Finnish)
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allele frequency: 6.880733944954129e-3
allele num: 6540
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Latino
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African
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Other
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InbreedingCoeff
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VQSLOD
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ClippingRankSum
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BaseQRankSum
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DP
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ReadPosRankSum
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FS
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MQ
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MQRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6558
num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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East Asian
type: Population
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Other
type: Population
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.553953257086027e-5
allele num: 64352
num of homozygotes: 0

South Asian
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allele frequency: 0.0e0
allele num: 15762
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 9936
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 7.36e0

FS
type: SiteQuality
SIO_000300: 3.344e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.415e0

MQRankSum
type: SiteQuality
SIO_000300: -4.69e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.800000000000001e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.1e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.859e0

VQSLOD
type: SiteQuality
SIO_000300: -1.082e0

DP
type: SiteQuality
SIO_000300: 1.608472e6

GenotypeQuality
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bin: 2.25e1
variant carriers: 1

GenotypeQuality
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bin: 5.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.5e0
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GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 3.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 2.75e1
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GenotypeQuality
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11092
num of homozygotes: 0

European (Non-Finnish)
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allele count: 7
allele frequency: 1.117996550182074e-4
allele num: 62612
num of homozygotes: 0

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

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

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8230
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

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.045e0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
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QD
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SIO_000300: 1.42e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

DP
type: SiteQuality
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ClippingRankSum
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SIO_000300: -5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.97e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 2

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11092
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6486
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.416014371872192e-5
allele num: 15586
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 6
allele frequency: 9.582827572989203e-5
allele num: 62612
num of homozygotes: 0

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

East Asian
type: Population
allele count: 2
allele frequency: 2.430133657351154e-4
allele num: 8230
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: -1.045e0

QD
type: SiteQuality
SIO_000300: 1.42e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.97e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -5.0e-2

MQRankSum
type: SiteQuality
SIO_000300: 6.3e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.88e0

DP
type: SiteQuality
SIO_000300: 1.648094e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.3e-3

GenotypeQuality
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variant carriers: 0

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

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

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8440
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.243756243756244e-5
allele num: 16016
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.82e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: -7.870000000000001e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.55e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.001e0

QD
type: SiteQuality
SIO_000300: 1.195e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.25e0

MQ
type: SiteQuality
SIO_000300: 5.883e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.3e-3

DP
type: SiteQuality
SIO_000300: 1.660687e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8450
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65470
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16036
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.936406995230525e-5
allele num: 10064
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11376
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.699999999999999e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.7e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 8.54e-1

MQRankSum
type: SiteQuality
SIO_000300: -3.55e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.28e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 7.67e-1

FS
type: SiteQuality
SIO_000300: 4.661e0

DP
type: SiteQuality
SIO_000300: 1.664791e6

QD
type: SiteQuality
SIO_000300: 1.475e1

GenotypeQuality
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variant carriers: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11406
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10092
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8468
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.523507724184162e-5
allele num: 65638
num of homozygotes: 0

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

Other
type: Population
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allele num: 882
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InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

ClippingRankSum
type: SiteQuality
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DP
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VQSLOD
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MQRankSum
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FS
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MQ
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BaseQRankSum
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SIO_000300: 3.63e-1

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

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

Latino
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allele count: 4
allele frequency: 3.502626970227671e-4
allele num: 11420
num of homozygotes: 0

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

South Asian
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: 888
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 65814
num of homozygotes: 0

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

European (Finnish)
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allele count: 1
allele frequency: 1.516530178950561e-4
allele num: 6594
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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Latino
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allele frequency: 0.0e0
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South Asian
type: Population
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Other
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66050
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African
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
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InbreedingCoeff
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FS
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BaseQRankSum
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QD
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MQRankSum
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ClippingRankSum
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DP
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ReadPosRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele count: 1
allele frequency: 9.8405825624877e-5
allele num: 10162
num of homozygotes: 0

East Asian
type: Population
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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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num of homozygotes: 0

European (Non-Finnish)
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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
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num of homozygotes: 0

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

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
SIO_000300: 1.707585e6

ClippingRankSum
type: SiteQuality
SIO_000300: -8.72e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: -5.1e-2

FS
type: SiteQuality
SIO_000300: 4.63e0

MQRankSum
type: SiteQuality
SIO_000300: 4.62e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.92e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

QD
type: SiteQuality
SIO_000300: 1.36e1

VQSLOD
type: SiteQuality
SIO_000300: 9.17e-1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

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

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

GenotypeQuality
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bin: 7.25e1
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GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.152331733727083e-5
allele num: 16254
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66250
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10190
num of homozygotes: 0

QD
type: SiteQuality
SIO_000300: 9.77e0

MQRankSum
type: SiteQuality
SIO_000300: -2.18e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.1e-2

VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.959e1

FS
type: SiteQuality
SIO_000300: 1.473e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 9.54e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 8.0e-2

DP
type: SiteQuality
SIO_000300: 1.714552e6

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66324
num of homozygotes: 0

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

African
type: Population
allele count: 3
allele frequency: 2.937720329024677e-4
allele num: 10212
num of homozygotes: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8578
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16266
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 6.0e1

VQSLOD
type: SiteQuality
SIO_000300: 1.51e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.323e0

MQRankSum
type: SiteQuality
SIO_000300: -3.16e-1

FS
type: SiteQuality
SIO_000300: 3.115e0

QD
type: SiteQuality
SIO_000300: 1.171e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.25e0

DP
type: SiteQuality
SIO_000300: 1.715897e6

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: 3.46e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16402
num of homozygotes: 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: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.676036786395974e-5
allele num: 11526
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10296
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66584
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: 1.24e0

DP
type: SiteQuality
SIO_000300: 1.730044e6

QD
type: SiteQuality
SIO_000300: 1.155e1

MQRankSum
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.67e-1

MQ
type: SiteQuality
SIO_000300: 5.917e1

VQSLOD
type: SiteQuality
SIO_000300: 8.3e-2

BaseQRankSum
type: SiteQuality
SIO_000300: -1.566e0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66604
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16418
num of homozygotes: 0

Latino
type: Population
allele count: 1
allele frequency: 8.671522719389525e-5
allele num: 11532
num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 6.62e-1

QD
type: SiteQuality
SIO_000300: 1.537e1

FS
type: SiteQuality
SIO_000300: 1.62e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.07e-1

DP
type: SiteQuality
SIO_000300: 1.731273e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.97e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQ
type: SiteQuality
SIO_000300: 5.853e1

MQRankSum
type: SiteQuality
SIO_000300: -8.72e-1

VQSLOD
type: SiteQuality
SIO_000300: -1.689e0

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: 681

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

Other
type: Population
allele count: 3
allele frequency: 3.333333333333334e-3
allele num: 900
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 568
allele frequency: 8.523921003661684e-3
allele num: 66636
num of homozygotes: 5

African
type: Population
allele count: 12
allele frequency: 1.163241566498643e-3
allele num: 10316
num of homozygotes: 0

South Asian
type: Population
allele count: 52
allele frequency: 3.164942178940961e-3
allele num: 16430
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 23
allele frequency: 3.480629539951574e-3
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 29
allele frequency: 2.51169236099082e-3
allele num: 11546
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.69e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.69e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -8.9e-2

FS
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 6.23e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.6e-3

DP
type: SiteQuality
SIO_000300: 1.756814e6

MQ
type: SiteQuality
SIO_000300: 5.976e1

QD
type: SiteQuality
SIO_000300: 1.242e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10316
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 900
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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16432
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500375093773443e-5
allele num: 66650
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: 1.42e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.762e0

FS
type: SiteQuality
SIO_000300: 9.57e-1

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
SIO_000300: 2.48e-1

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.833e1

QD
type: SiteQuality
SIO_000300: 1.242e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.084945843981989e-5
allele num: 16434
num of homozygotes: 0

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

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

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

Other
type: Population
allele count: 0
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allele num: 900
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BaseQRankSum
type: SiteQuality
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MQ
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ReadPosRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
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MQRankSum
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FS
type: SiteQuality
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VQSLOD
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DP
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QD
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.5004651441947e-5
allele num: 66646
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16434
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: 8.6e-1

MQRankSum
type: SiteQuality
SIO_000300: 5.16e-1

FS
type: SiteQuality
SIO_000300: 5.957e0

DP
type: SiteQuality
SIO_000300: 1.738118e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.81e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.83e-1

MQ
type: SiteQuality
SIO_000300: 5.933e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: 1.56e-1

QD
type: SiteQuality
SIO_000300: 1.452e1

GenotypeQuality
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bin: 4.75e1
variant carriers: 0

GenotypeQuality
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bin: 1.25e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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bin: 9.25e1
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GenotypeQuality
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bin: 6.25e1
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GenotypeQuality
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bin: 8.25e1
variant carriers: 0

GenotypeQuality
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bin: 2.25e1
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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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 64
bin: 3.25e1
variant carriers: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11554
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66662
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.085686465433301e-5
allele num: 16432
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.016e0

MQ
type: SiteQuality
SIO_000300: 5.875e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.194e0

QD
type: SiteQuality
SIO_000300: 1.119e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.21e0

MQRankSum
type: SiteQuality
SIO_000300: 3.5e-2

VQSLOD
type: SiteQuality
SIO_000300: -1.152e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.232e0

DP
type: SiteQuality
SIO_000300: 1.738596e6

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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bin: 2.5e0
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GenotypeQuality
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variant carriers: 1

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

GenotypeQuality
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bin: 8.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 9.691800736576855e-5
allele num: 10318
num of homozygotes: 0

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16414
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

BaseQRankSum
type: SiteQuality
SIO_000300: -1.711e0

DP
type: SiteQuality
SIO_000300: 1.736522e6

ClippingRankSum
type: SiteQuality
SIO_000300: -1.352e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.96e0

FS
type: SiteQuality
SIO_000300: 1.607e0

VQSLOD
type: SiteQuality
SIO_000300: -9.291e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.22e-1

MQ
type: SiteQuality
SIO_000300: 6.0e1

QD
type: SiteQuality
SIO_000300: 6.96e0

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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
all individuals: 5393
bin: 9.75e1
variant carriers: 2

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.001921229586936e-5
allele num: 66624
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10318
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16410
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.903e1

ClippingRankSum
type: SiteQuality
SIO_000300: -9.55e-1

FS
type: SiteQuality
SIO_000300: 3.527e0

VQSLOD
type: SiteQuality
SIO_000300: -1.028e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.69e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.21e-1

DP
type: SiteQuality
SIO_000300: 1.736188e6

QD
type: SiteQuality
SIO_000300: 1.403e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.82e0

GenotypeQuality
all individuals: 93
bin: 3.75e1
variant carriers: 0

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 2360
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GenotypeQuality
all individuals: 3594
bin: 7.75e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16398
num of homozygotes: 0

East Asian
type: Population
allele count: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10312
num of homozygotes: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66584
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.33e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

DP
type: SiteQuality
SIO_000300: 1.733404e6

QD
type: SiteQuality
SIO_000300: 7.49e0

BaseQRankSum
type: SiteQuality
SIO_000300: -2.018e0

MQRankSum
type: SiteQuality
SIO_000300: 9.340000000000001e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.534e0

VQSLOD
type: SiteQuality
SIO_000300: -6.251e-1

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

GenotypeQuality
all individuals: 150
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10298
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.006162633398467e-5
allele num: 66530
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

ClippingRankSum
type: SiteQuality
SIO_000300: -5.7e-2

FS
type: SiteQuality
SIO_000300: 2.95e0

MQRankSum
type: SiteQuality
SIO_000300: 2.86e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 8.34e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.0e-4

DP
type: SiteQuality
SIO_000300: 1.73592e6

QD
type: SiteQuality
SIO_000300: 3.328e1

BaseQRankSum
type: SiteQuality
SIO_000300: -2.39e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.08e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
all individuals: 230
bin: 2.75e1
variant carriers: 0

GenotypeQuality
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bin: 4.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.005530175522962e-5
allele num: 66544
num of homozygotes: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16376
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 8.66e-1

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 8.100000000000001e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

ReadPosRankSum
type: SiteQuality
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DP
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.933e1

BaseQRankSum
type: SiteQuality
SIO_000300: 3.19e0

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: 4.25e1
variant carriers: 0

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

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

East Asian
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allele frequency: 1.157139551029854e-4
allele num: 8642
num of homozygotes: 0

African
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66506
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Other
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allele frequency: 0.0e0
allele num: 900
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South Asian
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allele count: 0
allele frequency: 0.0e0
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MQ
type: SiteQuality
SIO_000300: 6.0e1

DP
type: SiteQuality
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QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
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BaseQRankSum
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e-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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bin: 9.75e1
variant carriers: 2

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.007428348019608e-5
allele num: 66502
num of homozygotes: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16358
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.832e1

VQSLOD
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QD
type: SiteQuality
SIO_000300: 1.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.32e0

FS
type: SiteQuality
SIO_000300: 2.974e0

DP
type: SiteQuality
SIO_000300: 1.716797e6

BaseQRankSum
type: SiteQuality
SIO_000300: -4.01e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.6e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 5.88e-1

GenotypeQuality
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bin: 2.5e0
variant carriers: 0

GenotypeQuality
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bin: 4.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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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: 40
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 5389
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505389293671343e-5
allele num: 66428
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16296
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10238
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.65e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.98e0

BaseQRankSum
type: SiteQuality
SIO_000300: 7.44e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

DP
type: SiteQuality
SIO_000300: 1.681828e6

VQSLOD
type: SiteQuality
SIO_000300: -2.366e0

QD
type: SiteQuality
SIO_000300: 1.814e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.76e-1

FS
type: SiteQuality
SIO_000300: 8.52e-1

MQ
type: SiteQuality
SIO_000300: 5.909e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

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: 16298
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.505570611261668e-5
allele num: 66420
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11522
num of homozygotes: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10250
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: 4.58e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.5e-2

MQRankSum
type: SiteQuality
SIO_000300: -3.08e-1

DP
type: SiteQuality
SIO_000300: 1.681668e6

BaseQRankSum
type: SiteQuality
SIO_000300: 2.19e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.9e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.86e-1

FS
type: SiteQuality
SIO_000300: 1.315e0

QD
type: SiteQuality
SIO_000300: 1.831e1

GenotypeQuality
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bin: 7.75e1
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 16268
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10222
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11514
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66392
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.159823706796567e-4
allele num: 8622
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: -6.62e-1

DP
type: SiteQuality
SIO_000300: 1.676096e6

FS
type: SiteQuality
SIO_000300: 1.042e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

ClippingRankSum
type: SiteQuality
SIO_000300: -1.2e-2

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.45e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.11e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 2.81e0

QD
type: SiteQuality
SIO_000300: 1.135e1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8604
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.507431637975218e-5
allele num: 66338
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16202
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 4.821e0

InbreedingCoeff
type: SiteQuality
SIO_000300: -8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -1.157e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.02e-1

QD
type: SiteQuality
SIO_000300: 1.14e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.86e0

VQSLOD
type: SiteQuality
SIO_000300: 3.29e-1

DP
type: SiteQuality
SIO_000300: 1.675027e6

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 9.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66322
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16192
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: 1
allele frequency: 9.807767752059631e-5
allele num: 10196
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6598
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8602
num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.11e-1

DP
type: SiteQuality
SIO_000300: 1.675277e6

FS
type: SiteQuality
SIO_000300: 0.0e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

MQRankSum
type: SiteQuality
SIO_000300: 2.08e-1

BaseQRankSum
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ClippingRankSum
type: SiteQuality
SIO_000300: -9.340000000000001e-1

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -9.0e-4

QD
type: SiteQuality
SIO_000300: 1.7e0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 8.75e1
variant carriers: 0

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

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 7500
num of homozygotes: 0

East Asian
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allele count: 0
allele frequency: 0.0e0
allele num: 132
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Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 118
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 3.695491500369549e-4
allele num: 2706
num of homozygotes: 0

MQ
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.304e0

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 1.89474e5

MQRankSum
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ReadPosRankSum
type: SiteQuality
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VQSLOD
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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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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num of homozygotes: 0

South Asian
type: Population
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allele frequency: 0.0e0
allele num: 7500
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 1
allele frequency: 3.695491500369549e-4
allele num: 2706
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.294e0

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
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QD
type: SiteQuality
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VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 5.590000000000001e-1

MQRankSum
type: SiteQuality
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DP
type: SiteQuality
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GenotypeQuality
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variant carriers: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 92
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 2708
num of homozygotes: 0

East Asian
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allele frequency: 0.0e0
allele num: 132
num of homozygotes: 0

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

South Asian
type: Population
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allele frequency: 1.333333333333333e-4
allele num: 7500
num of homozygotes: 0

Other
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num of homozygotes: 0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.15e0

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 188
num of homozygotes: 0

South Asian
type: Population
allele count: 1
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East Asian
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Latino
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Other
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European (Finnish)
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QD
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ClippingRankSum
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MQ
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BaseQRankSum
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FS
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VQSLOD
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DP
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MQRankSum
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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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GenotypeQuality
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Latino
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Other
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East Asian
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European (Non-Finnish)
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African
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allele frequency: 0.0e0
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European (Finnish)
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InbreedingCoeff
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DP
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ClippingRankSum
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FS
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MQ
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VQSLOD
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BaseQRankSum
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MQRankSum
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QD
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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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European (Non-Finnish)
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European (Finnish)
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East Asian
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South Asian
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Latino
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African
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Other
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VQSLOD
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FS
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BaseQRankSum
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ReadPosRankSum
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ClippingRankSum
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InbreedingCoeff
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DP
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MQRankSum
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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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East Asian
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African
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Latino
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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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VQSLOD
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FS
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MQRankSum
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ClippingRankSum
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InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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QD
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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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South Asian
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allele num: 16306
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African
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East Asian
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Other
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European (Finnish)
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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ReadPosRankSum
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MQ
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InbreedingCoeff
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MQRankSum
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QD
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VQSLOD
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BaseQRankSum
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ClippingRankSum
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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
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European (Finnish)
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Other
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African
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East Asian
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Latino
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European (Non-Finnish)
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ReadPosRankSum
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FS
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VQSLOD
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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DP
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ClippingRankSum
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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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Latino
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European (Non-Finnish)
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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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MQRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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FS
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MQ
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QD
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InbreedingCoeff
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ReadPosRankSum
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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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European (Non-Finnish)
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Latino
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South Asian
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European (Finnish)
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African
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QD
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ClippingRankSum
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MQ
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BaseQRankSum
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ReadPosRankSum
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FS
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InbreedingCoeff
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DP
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MQRankSum
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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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Latino
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Other
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European (Non-Finnish)
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East Asian
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South Asian
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African
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European (Finnish)
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VQSLOD
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DP
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FS
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MQ
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MQRankSum
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QD
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BaseQRankSum
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InbreedingCoeff
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ClippingRankSum
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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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African
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South Asian
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European (Finnish)
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Latino
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Other
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European (Non-Finnish)
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East Asian
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DP
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InbreedingCoeff
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BaseQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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MQRankSum
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FS
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 9.75e1
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 6330
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502494140272853e-5
allele num: 66556
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: 0
allele frequency: 0.0e0
allele num: 9966
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16478
num of homozygotes: 0

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

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.693e0

MQRankSum
type: SiteQuality
SIO_000300: 6.18e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 2.59e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.62e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.74e-1

QD
type: SiteQuality
SIO_000300: 1.353e1

VQSLOD
type: SiteQuality
SIO_000300: -7.558e-1

DP
type: SiteQuality
SIO_000300: 3.221447e6

MQ
type: SiteQuality
SIO_000300: 6.0e1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.003814495081309e-4
allele num: 9962
num of homozygotes: 0

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

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

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

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 3.004897983713453e-5
allele num: 66558
num of homozygotes: 0

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

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

BaseQRankSum
type: SiteQuality
SIO_000300: -2.234e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.77e-1

MQRankSum
type: SiteQuality
SIO_000300: 3.52e-1

QD
type: SiteQuality
SIO_000300: 1.079e1

FS
type: SiteQuality
SIO_000300: 3.731e0

VQSLOD
type: SiteQuality
SIO_000300: 1.61e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 9.9e-2

InbreedingCoeff
type: SiteQuality
SIO_000300: -4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.937e1

DP
type: SiteQuality
SIO_000300: 3.221569e6

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
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GenotypeQuality
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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: 60
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variant carriers: 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: 8648
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9900
num of homozygotes: 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: 6610
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502584445245823e-5
allele num: 66552
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -1.81e0

FS
type: SiteQuality
SIO_000300: 1.635e0

VQSLOD
type: SiteQuality
SIO_000300: 3.48e0

DP
type: SiteQuality
SIO_000300: 3.218344e6

MQRankSum
type: SiteQuality
SIO_000300: -1.63e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.15e-1

MQ
type: SiteQuality
SIO_000300: 5.78e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -2.03e-1

QD
type: SiteQuality
SIO_000300: 1.426e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -5.999999999999999e-4

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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bin: 5.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9874
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502855425308085e-5
allele num: 66540
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -3.232e-1

DP
type: SiteQuality
SIO_000300: 3.217378e6

QD
type: SiteQuality
SIO_000300: 1.242e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -3.421e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.422e0

MQ
type: SiteQuality
SIO_000300: 5.928e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.52e0

MQRankSum
type: SiteQuality
SIO_000300: 8.72e-1

FS
type: SiteQuality
SIO_000300: 3.087e0

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 1581
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variant carriers: 0

GenotypeQuality
all individuals: 77
bin: 2.75e1
variant carriers: 0

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66550
num of homozygotes: 0

African
type: Population
allele count: 2
allele frequency: 2.026753141467369e-4
allele num: 9868
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 7.0e-4

FS
type: SiteQuality
SIO_000300: 1.825e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.27e0

QD
type: SiteQuality
SIO_000300: 1.556e1

DP
type: SiteQuality
SIO_000300: 3.216929e6

MQRankSum
type: SiteQuality
SIO_000300: 4.36e-1

MQ
type: SiteQuality
SIO_000300: 5.964e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.28e0

VQSLOD
type: SiteQuality
SIO_000300: 1.66e0

ClippingRankSum
type: SiteQuality
SIO_000300: -3.25e-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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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9872
num of homozygotes: 0

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66542
num of homozygotes: 0

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

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 4.7e-2

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -8.19e-1

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
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VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.0e-4

MQ
type: SiteQuality
SIO_000300: 5.958e1

QD
type: SiteQuality
SIO_000300: 2.931e1

GenotypeQuality
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variant carriers: 0

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

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

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

European (Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 6608
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11556
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9870
num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 3.005710850616171e-5
allele num: 66540
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
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MQRankSum
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MQ
type: SiteQuality
SIO_000300: 5.981e1

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

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 16496
num of homozygotes: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.502765087761481e-5
allele num: 66544
num of homozygotes: 0

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9864
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11552
num of homozygotes: 0

European (Finnish)
type: Population
allele count: 1
allele frequency: 1.513775355737209e-4
allele num: 6606
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 904
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MQ
type: SiteQuality
SIO_000300: 5.436e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

MQRankSum
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DP
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QD
type: SiteQuality
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FS
type: SiteQuality
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VQSLOD
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ClippingRankSum
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 9868
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
allele num: 6608
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Latino
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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: 8646
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European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.502358703163967e-5
allele num: 66562
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South Asian
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DP
type: SiteQuality
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FS
type: SiteQuality
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QD
type: SiteQuality
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MQRankSum
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VQSLOD
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MQ
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InbreedingCoeff
type: SiteQuality
SIO_000300: 6.2e-3

BaseQRankSum
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ClippingRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 6.75e1
variant carriers: 0

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

East Asian
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allele frequency: 0.0e0
allele num: 8648
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African
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allele count: 0
allele frequency: 0.0e0
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Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11550
num of homozygotes: 0

European (Finnish)
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allele count: 0
allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
allele num: 16498
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.9e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.35e0

MQ
type: SiteQuality
SIO_000300: 6.0e1

MQRankSum
type: SiteQuality
SIO_000300: 7.08e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.18e0

VQSLOD
type: SiteQuality
SIO_000300: -1.518e-1

FS
type: SiteQuality
SIO_000300: 7.823e0

QD
type: SiteQuality
SIO_000300: 1.44e1

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.53e-1

DP
type: SiteQuality
SIO_000300: 3.213852e6

GenotypeQuality
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bin: 2.75e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 1.75e1
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GenotypeQuality
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bin: 3.25e1
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GenotypeQuality
all individuals: 2635
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2887
bin: 9.25e1
variant carriers: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16498
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: 9874
num of homozygotes: 0

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

East Asian
type: Population
allele count: 1
allele frequency: 1.156871818602499e-4
allele num: 8644
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66564
num of homozygotes: 0

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

VQSLOD
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 8.42e-1

DP
type: SiteQuality
SIO_000300: 3.214816e6

FS
type: SiteQuality
SIO_000300: 0.0e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.874e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.5e-3

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: -7.5e-2

QD
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SIO_000300: 1.201e1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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: 116

GenotypeQuality
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variant carriers: 0

South Asian
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allele count: 119
allele frequency: 7.212995514607831e-3
allele num: 16498
num of homozygotes: 5

Latino
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allele count: 0
allele frequency: 0.0e0
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African
type: Population
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Other
type: Population
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allele frequency: 1.106194690265487e-3
allele num: 904
num of homozygotes: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.50195253829979e-5
allele num: 66580
num of homozygotes: 0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.89e-1

QD
type: SiteQuality
SIO_000300: 1.692e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.41e-2

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

DP
type: SiteQuality
SIO_000300: 3.218345e6

FS
type: SiteQuality
SIO_000300: 5.38e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.84e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.73e-1

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
all individuals: 6562
bin: 6.25e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500420117632937e-5
allele num: 66648
num of homozygotes: 0

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11564
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: 8646
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10030
num of homozygotes: 0

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

DP
type: SiteQuality
SIO_000300: 3.220121e6

ReadPosRankSum
type: SiteQuality
SIO_000300: -3.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 9.0e-4

FS
type: SiteQuality
SIO_000300: 1.9169e1

MQRankSum
type: SiteQuality
SIO_000300: -2.096e0

MQ
type: SiteQuality
SIO_000300: 5.952e1

VQSLOD
type: SiteQuality
SIO_000300: -3.113e0

QD
type: SiteQuality
SIO_000300: 1.432e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.513e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.65e-1

GenotypeQuality
all individuals: 5
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variant carriers: 0

GenotypeQuality
all individuals: 2893
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
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variant carriers: 0

GenotypeQuality
all individuals: 15
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GenotypeQuality
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GenotypeQuality
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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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.500240038406145e-5
allele num: 66656
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10084
num of homozygotes: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11568
num of homozygotes: 0

VQSLOD
type: SiteQuality
SIO_000300: -9.727e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.174e0

ClippingRankSum
type: SiteQuality
SIO_000300: -7.73e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.22e-1

FS
type: SiteQuality
SIO_000300: 1.0564e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 8.0e-4

MQRankSum
type: SiteQuality
SIO_000300: 1.2e0

MQ
type: SiteQuality
SIO_000300: 5.981e1

QD
type: SiteQuality
SIO_000300: 1.099e1

DP
type: SiteQuality
SIO_000300: 3.220971e6

GenotypeQuality
all individuals: 1583
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 2580
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
all individuals: 24
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GenotypeQuality
all individuals: 35
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GenotypeQuality
all individuals: 7
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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: 2672
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40113
bin: 9.75e1
variant carriers: 1

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66660
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11572
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: 16500
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10100
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: 1
allele frequency: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.22115e6

ClippingRankSum
type: SiteQuality
SIO_000300: 1.16e0

VQSLOD
type: SiteQuality
SIO_000300: -1.287e-1

MQ
type: SiteQuality
SIO_000300: 5.94e1

QD
type: SiteQuality
SIO_000300: 1.398e1

FS
type: SiteQuality
SIO_000300: 0.0e0

MQRankSum
type: SiteQuality
SIO_000300: -5.01e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.2e-3

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.256e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.391e0

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
all individuals: 11
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variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10148
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999760019198464e-5
allele num: 66672
num of homozygotes: 0

Latino
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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: 8646
num of homozygotes: 0

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

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

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

MQRankSum
type: SiteQuality
SIO_000300: 5.47e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.79e-1

FS
type: SiteQuality
SIO_000300: 5.81e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

VQSLOD
type: SiteQuality
SIO_000300: 3.16e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

BaseQRankSum
type: SiteQuality
SIO_000300: -2.08e0

DP
type: SiteQuality
SIO_000300: 3.221985e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.22e-1

QD
type: SiteQuality
SIO_000300: 1.294e1

GenotypeQuality
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bin: 6.75e1
variant carriers: 0

GenotypeQuality
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bin: 7.75e1
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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variant carriers: 0

GenotypeQuality
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bin: 6.25e1
variant carriers: 0

European (Finnish)
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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: 16500
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 2
allele frequency: 2.999760019198464e-5
allele num: 66672
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: 1
allele frequency: 9.854158454867954e-5
allele num: 10148
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: 1.156604210039325e-4
allele num: 8646
num of homozygotes: 0

FS
type: SiteQuality
SIO_000300: 5.81e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.5e-3

MQRankSum
type: SiteQuality
SIO_000300: 5.47e-1

MQ
type: SiteQuality
SIO_000300: 5.978e1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 7.22e-1

VQSLOD
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ClippingRankSum
type: SiteQuality
SIO_000300: -6.79e-1

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -2.08e0

GenotypeQuality
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variant carriers: 0

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

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

East Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 8646
num of homozygotes: 0

European (Non-Finnish)
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allele count: 2
allele frequency: 2.999670036296008e-5
allele num: 66674
num of homozygotes: 0

African
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Other
type: Population
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allele num: 906
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Latino
type: Population
allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.149e0

QD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: 4.51e0

ClippingRankSum
type: SiteQuality
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MQRankSum
type: SiteQuality
SIO_000300: 8.63e-1

MQ
type: SiteQuality
SIO_000300: 5.987e1

DP
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 8.19e-1

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 21

GenotypeQuality
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GenotypeQuality
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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: 2892
bin: 9.25e1
variant carriers: 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: 10204
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66680
num of homozygotes: 0

South Asian
type: Population
allele count: 0
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East Asian
type: Population
allele count: 22
allele frequency: 2.544529262086514e-3
allele num: 8646
num of homozygotes: 1

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11574
num of homozygotes: 0

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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ReadPosRankSum
type: SiteQuality
SIO_000300: 6.75e-1

MQRankSum
type: SiteQuality
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FS
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SIO_000300: 0.0e0

DP
type: SiteQuality
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VQSLOD
type: SiteQuality
SIO_000300: 5.05e0

InbreedingCoeff
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.979e1

QD
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SIO_000300: 1.389e1

ClippingRankSum
type: SiteQuality
SIO_000300: -6.929999999999999e-1