8-146067797-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067797
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067797
    reference: chr 8
allele count: 2
allele frequency: 1.680135754969001e-5
allele num: 119038
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1305C>T
  hgvsp: ENST00000325241.6:c.1305C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3567C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1338C>T
  hgvsp: ENST00000446747.2:c.1338C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4833C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-669G>A
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1017C>T
  hgvsp: ENST00000544249.1:c.1017C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1305C>T
  hgvsp: ENST00000528372.1:c.1305C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3567C>T
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 503
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1033
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 4.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 216
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2898
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 156
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His435His
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: QD

8-146067802-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067802
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067802
    reference: chr 8
allele count: 1
allele frequency: 8.3948959032908e-6
allele num: 119120
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1343G>A
  hgvsp: ENSP00000393260.2:p.Gly448Glu
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-674C>T
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3562G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3562G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1310G>A
  hgvsp: ENSP00000432724.1:p.Gly437Glu
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4838G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1310G>A
  hgvsp: ENSP00000320627.6:p.Gly437Glu
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1022G>A
  hgvsp: ENSP00000439424.1:p.Gly341Glu
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 495
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 200
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2912
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3015
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2951
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1018
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 112
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6376
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1309
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 9
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1843
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 118
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Gly437Glu
num of homozygotes: 0
population: South Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
population: Other
population: African
reference allele: G
site quality: MQ
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

8-146067809-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067809
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067809
    reference: chr 8
allele count: 1
allele frequency: 8.383916294979712e-6
allele num: 119276
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-681C>T
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3555G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1029G>A
  hgvsp: ENST00000544249.1:c.1029G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1317G>A
  hgvsp: ENST00000528372.1:c.1317G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1317G>A
  hgvsp: ENST00000325241.6:c.1317G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3555G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1350G>A
  hgvsp: ENST00000446747.2:c.1350G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4845G>A
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3021
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 456
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 978
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 209
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 728
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2960
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3010
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 70
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4263
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6376
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1845
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 133
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1571
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 134
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 95
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5318
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Lys439Lys
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: South Asian
population: Other
population: East Asian
population: European (Finnish)
reference allele: G
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: QD

8-146067827-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067827
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067827
    reference: chr 8
allele count: 1
allele frequency: 8.355056480181806e-6
allele num: 119688
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1368G>A
  hgvsp: ENST00000446747.2:c.1368G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3537G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4863G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1335G>A
  hgvsp: ENST00000528372.1:c.1335G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1335G>A
  hgvsp: ENST00000325241.6:c.1335G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1047G>A
  hgvsp: ENST00000544249.1:c.1047G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3537G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-699C>T
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3051
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4262
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3229
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 378
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6376
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5880
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 161
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 827
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3032
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1845
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 68
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2164
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1624
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 121
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Lys445Lys
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
population: Other
population: African
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: DP
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: ReadPosRankSum

8-146067834-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067834
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067834
    reference: chr 8
allele count: 1
allele frequency: 8.339448929214757e-6
allele num: 119912
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4870A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1054A>G
  hgvsp: ENSP00000439424.1:p.Lys352Glu
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1375A>G
  hgvsp: ENSP00000393260.2:p.Lys459Glu
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-706T>C
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1342A>G
  hgvsp: ENSP00000320627.6:p.Lys448Glu
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1342A>G
  hgvsp: ENSP00000432724.1:p.Lys448Glu
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3530A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3530A>G
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6376
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 320
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3084
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 11
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3038
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3384
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1846
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 104
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 53
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys448Glu
num of homozygotes: 0
population: African
population: Latino
population: Other
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: BaseQRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: DP
site quality: ClippingRankSum

http://identifiers.org/exac.variant/8-146067835-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067835
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067835
    reference: chr 8
allele count: 1
allele frequency: 8.33541718763024e-6
allele num: 119970
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-707T>G
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1376A>C
  hgvsp: ENSP00000393260.2:p.Lys459Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1343A>C
  hgvsp: ENSP00000432724.1:p.Lys448Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3529A>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4871A>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1343A>C
  hgvsp: ENSP00000320627.6:p.Lys448Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1055A>C
  hgvsp: ENSP00000439424.1:p.Lys352Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3529A>C
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3037
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 707
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3990
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3412
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 310
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 130
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3097
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5811
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1625
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1930
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 97
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Lys448Thr
num of homozygotes: 0
population: South Asian
population: African
population: European (Finnish)
population: Other
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: DP
site quality: MQRankSum
site quality: MQ
site quality: VQSLOD
site quality: ClippingRankSum

8-146067837-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067837
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067837
    reference: chr 8
allele count: 1
allele frequency: 8.331389342486753e-6
allele num: 120028
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4873G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1345G>A
  hgvsp: ENSP00000432724.1:p.Ala449Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-709C>T
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1378G>A
  hgvsp: ENSP00000393260.2:p.Ala460Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3527G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1345G>A
  hgvsp: ENSP00000320627.6:p.Ala449Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3527G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1057G>A
  hgvsp: ENSP00000439424.1:p.Ala353Thr
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3099
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3040
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 673
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 300
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3438
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 142
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 94
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5779
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 106
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 56
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ala449Thr
num of homozygotes: 0
population: African
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: East Asian
reference allele: G
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-146067838-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067838
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067838
    reference: chr 8
allele count: 1
allele frequency: 8.328475056217207e-6
allele num: 120070
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3526C>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1346C>A
  hgvsp: ENSP00000432724.1:p.Ala449Asp
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4874C>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1058C>A
  hgvsp: ENSP00000439424.1:p.Ala353Asp
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3526C>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1379C>A
  hgvsp: ENSP00000393260.2:p.Ala460Asp
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1346C>A
  hgvsp: ENSP00000320627.6:p.Ala449Asp
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-710G>T
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 287
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3042
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3101
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 658
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3466
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 8
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6376
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 90
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1923
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ala449Asp
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-146067846-TGTA-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067846
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067843
    reference: chr 8
allele count: 1
allele frequency: 8.310203267571925e-6
allele num: 120334
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-721_*117-719delTAC
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1069_1071delAGT
  hgvsp: ENSP00000439424.1:p.Ser357del
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3515_248-3513delAGT
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1390_1392delAGT
  hgvsp: ENSP00000393260.2:p.Ser464del
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: inframe_deletion
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1357_1359delAGT
  hgvsp: ENSP00000432724.1:p.Ser453del
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: inframe_deletion
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1357_1359delAGT
  hgvsp: ENSP00000320627.6:p.Ser453del
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4885_4887delAGT
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3515_281-3513delAGT
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: inframe deletion
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 533
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 238
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3173
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 991
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4268
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3054
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 137
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7154
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 81
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 641
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5939
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ser453del
num of homozygotes: 0
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: TGTA
site quality: BaseQRankSum
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: MQRankSum
site quality: FS
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD

8-146067855-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067855
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067855
    reference: chr 8
allele count: 1
allele frequency: 8.292011476143882e-6
allele num: 120598
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1396C>T
  hgvsp: ENSP00000393260.2:p.Arg466Trp
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1075C>T
  hgvsp: ENSP00000439424.1:p.Arg359Trp
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-727G>A
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3509C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1363C>T
  hgvsp: ENSP00000432724.1:p.Arg455Trp
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4891C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3509C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1363C>T
  hgvsp: ENSP00000320627.6:p.Arg455Trp
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 399
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3691
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3252
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3059
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 182
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1947
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43179
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1852
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 69
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 89
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1575
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Arg455Trp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: Other
population: European (Non-Finnish)
population: Latino
population: South Asian
population: African
reference allele: C
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: FS
site quality: ClippingRankSum

8-146067857-GC-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067857
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067856
    reference: chr 8
allele count: 1
allele frequency: 8.280476292996373e-6
allele num: 120766
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3506delC
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4894delC
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3506delC
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1366delC
  hgvsp: ENSP00000320627.6:p.Ile457PhefsTer80
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1399delC
  hgvsp: ENSP00000393260.2:p.Ile468PhefsTer80
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1078delC
  hgvsp: ENSP00000439424.1:p.Ile361PhefsTer80
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-730delG
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1366delC
  hgvsp: ENSP00000432724.1:p.Ile457PhefsTer80
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3068
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4266
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 158
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3302
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7154
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 314
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 48
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 5
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Ile457PhefsTer80
num of homozygotes: 0
population: Latino
population: South Asian
population: European (Non-Finnish)
population: African
population: European (Finnish)
population: Other
population: East Asian
reference allele: GC
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: DP

8-146067862-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067862
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067862
    reference: chr 8
allele count: 1
allele frequency: 8.272256506129742e-6
allele num: 120886
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1403T>C
  hgvsp: ENSP00000393260.2:p.Ile468Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1370T>C
  hgvsp: ENSP00000432724.1:p.Ile457Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1370T>C
  hgvsp: ENSP00000320627.6:p.Ile457Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-734A>G
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1082T>C
  hgvsp: ENSP00000439424.1:p.Ile361Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3502T>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4898T>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3502T>C
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3327
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4265
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1926
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 140
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3803
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3069
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 729
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 261
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 63
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 52
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Ile457Thr
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

8-146067864-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067864
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067864
    reference: chr 8
allele count: 2
allele frequency: 1.654177625593436e-5
allele num: 120906
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1084C>T
  hgvsp: ENSP00000439424.1:p.Arg362Cys
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-736G>A
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3500C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1372C>T
  hgvsp: ENSP00000432724.1:p.Arg458Cys
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1405C>T
  hgvsp: ENSP00000393260.2:p.Arg469Cys
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1372C>T
  hgvsp: ENSP00000320627.6:p.Arg458Cys
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3500C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4900C>T
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3071
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 247
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3783
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4264
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7155
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6977
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1927
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3354
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 139
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 55
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1984
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1345
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 49
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Arg458Cys
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
population: South Asian
reference allele: C
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum

8-146067865-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067865
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067865
    reference: chr 8
allele count: 2
allele frequency: 1.653767281868095e-5
allele num: 120936
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3499G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4901G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1406G>A
  hgvsp: ENSP00000393260.2:p.Arg469His
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1085G>A
  hgvsp: ENSP00000439424.1:p.Arg362His
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-737C>T
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1373G>A
  hgvsp: ENSP00000432724.1:p.Arg458His
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3499G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1373G>A
  hgvsp: ENSP00000320627.6:p.Arg458His
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 229
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3079
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2055
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 132
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3358
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1975
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 294
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Arg458His
num of homozygotes: 0
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: African
population: South Asian
reference allele: G
site quality: MQ
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: QD
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff

8-146067878-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067878
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067878
    reference: chr 8
allele count: 1
allele frequency: 8.251233559417133e-6
allele num: 121194
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3486T>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1386T>C
  hgvsp: ENST00000528372.1:c.1386T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1386T>C
  hgvsp: ENST00000325241.6:c.1386T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1098T>C
  hgvsp: ENST00000544249.1:c.1098T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4914T>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3486T>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1419T>C
  hgvsp: ENST00000446747.2:c.1419T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-750A>G
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 106
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3896
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4267
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3076
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3431
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6546
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 54
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 152
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Thr462Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Latino
population: East Asian
population: South Asian
population: Other
population: European (Finnish)
reference allele: T
site quality: ReadPosRankSum
site quality: FS
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ClippingRankSum
site quality: DP
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD

8-146067881-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067881
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067881
    reference: chr 8
allele count: 1
allele frequency: 8.250144377526608e-6
allele num: 121210
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1389C>T
  hgvsp: ENST00000325241.6:c.1389C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1422C>T
  hgvsp: ENST00000446747.2:c.1422C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1101C>T
  hgvsp: ENST00000544249.1:c.1101C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-753G>A
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4917C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1389C>T
  hgvsp: ENST00000528372.1:c.1389C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3483C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3483C>T
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3078
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 97
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3448
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3991
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5878
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3895
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 7.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1854
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 57
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2016
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.His463His
num of homozygotes: 0
population: East Asian
population: Other
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: QD
site quality: MQ
site quality: DP

http://identifiers.org/exac.variant/8-146067894-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067894
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067894
    reference: chr 8
allele count: 1
allele frequency: 8.242664029014178e-6
allele num: 121320
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-766G>T
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1402C>A
  hgvsp: ENSP00000432724.1:p.Pro468Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1402C>A
  hgvsp: ENSP00000320627.6:p.Pro468Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1114C>A
  hgvsp: ENSP00000439424.1:p.Pro372Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3470C>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1435C>A
  hgvsp: ENSP00000393260.2:p.Pro479Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4930C>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3470C>A
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3081
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 44
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3484
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3913
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6977
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1860
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43184
  bin: 9.75e1
  variant carriers: 1
hgvs: p.Pro468Thr
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: MQ
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD

8-146067898-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067898
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067898
    reference: chr 8
allele count: 1
allele frequency: 8.242392271933006e-6
allele num: 121324
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1406T>C
  hgvsp: ENSP00000320627.6:p.Phe469Ser
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3466T>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-770A>G
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1439T>C
  hgvsp: ENSP00000393260.2:p.Phe480Ser
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1406T>C
  hgvsp: ENSP00000432724.1:p.Phe469Ser
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4934T>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3466T>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1118T>C
  hgvsp: ENSP00000439424.1:p.Phe373Ser
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1433
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 43
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3083
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 77
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 102
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3907
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3474
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6979
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1349
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Phe469Ser
num of homozygotes: 0
population: European (Finnish)
population: East Asian
population: African
population: South Asian
population: European (Non-Finnish)
population: Latino
population: Other
reference allele: T
site quality: MQRankSum
site quality: QD
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: VQSLOD
site quality: DP
site quality: ReadPosRankSum

8-146067910-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067910
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067910
    reference: chr 8
allele count: 4
allele frequency: 3.296033224014898e-5
allele num: 121358
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3454A>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1451A>T
  hgvsp: ENSP00000393260.2:p.Glu484Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1418A>T
  hgvsp: ENSP00000320627.6:p.Glu473Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-782T>A
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4946A>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1418A>T
  hgvsp: ENSP00000432724.1:p.Glu473Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1130A>T
  hgvsp: ENSP00000439424.1:p.Glu377Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3454A>T
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 7.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6978
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3502
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1929
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3091
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3881
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6601
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1348
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Glu473Val
num of homozygotes: 0
population: East Asian
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: South Asian
population: European (Finnish)
reference allele: A
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: BaseQRankSum

8-146067913-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067913
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067913
    reference: chr 8
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-785C>T
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1421G>A
  hgvsp: ENSP00000320627.6:p.Cys474Tyr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3451G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1133G>A
  hgvsp: ENSP00000439424.1:p.Cys378Tyr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3451G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1454G>A
  hgvsp: ENSP00000393260.2:p.Cys485Tyr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1421G>A
  hgvsp: ENSP00000432724.1:p.Cys474Tyr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4949G>A
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 27
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1928
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3882
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3506
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5879
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6979
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2171
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1637
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 66
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Cys474Tyr
num of homozygotes: 0
population: East Asian
population: South Asian
population: Other
population: Latino
population: European (Finnish)
population: European (Non-Finnish)
population: African
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: QD

8-146067917-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067917
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067917
    reference: chr 8
allele count: 3
allele frequency: 2.47222863170386e-5
allele num: 121348
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1425C>G
  hgvsp: ENST00000528372.1:c.1425C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3447C>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4953C>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1137C>G
  hgvsp: ENST00000544249.1:c.1137C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3447C>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1425C>G
  hgvsp: ENST00000325241.6:c.1425C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1458C>G
  hgvsp: ENST00000446747.2:c.1458C>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-789G>C
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 104
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3876
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3507
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6981
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3087
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6609
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2171
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2009
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly475Gly
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: Latino
population: South Asian
population: African
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: QD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: DP

8-146067919-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067919
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067919
    reference: chr 8
allele count: 1
allele frequency: 8.239947264337508e-6
allele num: 121360
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4955A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1139A>G
  hgvsp: ENSP00000439424.1:p.Lys380Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3445A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1460A>G
  hgvsp: ENSP00000393260.2:p.Lys487Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3445A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1427A>G
  hgvsp: ENSP00000320627.6:p.Lys476Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1427A>G
  hgvsp: ENSP00000432724.1:p.Lys476Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-791T>C
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3871
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3093
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 25
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6977
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3512
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 103
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1646
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6618
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys476Arg
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Latino
population: Other
population: East Asian
reference allele: A
site quality: MQRankSum
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ

8-146067932-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067932
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067932
    reference: chr 8
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1440G>A
  hgvsp: ENST00000528372.1:c.1440G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-804C>T
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1152G>A
  hgvsp: ENST00000544249.1:c.1152G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1440G>A
  hgvsp: ENST00000325241.6:c.1440G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3432G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1473G>A
  hgvsp: ENST00000446747.2:c.1473G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3432G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4968G>A
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 24
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3098
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3515
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3856
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 730
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43190
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 67
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1357
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1853
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Gln480Gln
num of homozygotes: 0
population: Other
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: Latino
population: South Asian
reference allele: G
site quality: MQ
site quality: MQRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: QD

8-146067942-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067942
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067942
    reference: chr 8
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1162C>G
  hgvsp: ENSP00000439424.1:p.Leu388Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1450C>G
  hgvsp: ENSP00000432724.1:p.Leu484Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1483C>G
  hgvsp: ENSP00000393260.2:p.Leu495Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-814G>C
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1450C>G
  hgvsp: ENSP00000320627.6:p.Leu484Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3422C>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4978C>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3422C>G
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3116
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3525
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3842
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3106
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1858
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 5.25e1
  variant carriers: 0
hgvs: p.Leu484Val
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: C
site quality: QD
site quality: DP
site quality: VQSLOD
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQRankSum
site quality: FS
site quality: ReadPosRankSum

8-146067950-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067950
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067950
    reference: chr 8
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1458G>A
  hgvsp: ENST00000325241.6:c.1458G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3414G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3414G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1458G>A
  hgvsp: ENST00000528372.1:c.1458G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1491G>A
  hgvsp: ENST00000446747.2:c.1491G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-822C>T
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4986G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1170G>A
  hgvsp: ENST00000544249.1:c.1170G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1639
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1578
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1361
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6593
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Gln486Gln
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-146067950-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067950
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067950
    reference: chr 8
allele count: 1
allele frequency: 8.240490473993011e-6
allele num: 121352
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1491G>C
  hgvsp: ENSP00000393260.2:p.Gln497His
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1458G>C
  hgvsp: ENSP00000320627.6:p.Gln486His
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3414G>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4986G>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1458G>C
  hgvsp: ENSP00000432724.1:p.Gln486His
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3414G>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1170G>C
  hgvsp: ENSP00000439424.1:p.Gln390His
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-822C>G
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3109
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 108
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3533
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4277
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3118
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2017
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
hgvs: p.Gln486His
num of homozygotes: 0
population: East Asian
population: South Asian
population: European (Non-Finnish)
population: African
population: Latino
population: Other
population: European (Finnish)
reference allele: G
site quality: ClippingRankSum
site quality: FS
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: DP

8-146067957-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067957
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067957
    reference: chr 8
allele count: 1
allele frequency: 8.240218860212928e-6
allele num: 121356
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4993C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1465C>T
  hgvsp: ENSP00000320627.6:p.Arg489Ter
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3407C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-829G>A
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1465C>T
  hgvsp: ENSP00000432724.1:p.Arg489Ter
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1498C>T
  hgvsp: ENSP00000393260.2:p.Arg500Ter
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1177C>T
  hgvsp: ENSP00000439424.1:p.Arg393Ter
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3407C>T
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 99
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3818
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3531
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5891
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5115
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1859
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 51
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Arg489Ter
num of homozygotes: 0
population: East Asian
population: African
population: South Asian
population: Other
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: BaseQRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQ
site quality: FS
site quality: QD
site quality: ClippingRankSum

8-146067958-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067958
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067958
    reference: chr 8
allele count: 2
allele frequency: 1.647907980818351e-5
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1466G>A
  hgvsp: ENSP00000432724.1:p.Arg489Gln
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3406G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3406G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4994G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-830C>T
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1466G>A
  hgvsp: ENSP00000320627.6:p.Arg489Gln
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1178G>A
  hgvsp: ENSP00000439424.1:p.Arg393Gln
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1499G>A
  hgvsp: ENSP00000393260.2:p.Arg500Gln
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3824
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5116
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6974
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 58
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2033
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2171
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Arg489Gln
num of homozygotes: 0
population: South Asian
population: African
population: East Asian
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: Other
reference allele: G
site quality: VQSLOD
site quality: DP
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: ClippingRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-146067962-C-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067962
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067962
    reference: chr 8
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3402C>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.4998C>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1182C>A
  hgvsp: ENST00000544249.1:c.1182C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1470C>A
  hgvsp: ENST00000528372.1:c.1470C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1503C>A
  hgvsp: ENST00000446747.2:c.1503C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3402C>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1470C>A
  hgvsp: ENST00000325241.6:c.1470C>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-834G>T
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7152
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3537
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3827
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6610
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ile490Ile
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: Other
population: Latino
population: South Asian
population: East Asian
population: European (Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: FS
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ

8-146067965-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067965
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067965
    reference: chr 8
allele count: 3
allele frequency: 2.471821237888076e-5
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3399C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5001C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1185C>T
  hgvsp: ENST00000544249.1:c.1185C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1473C>T
  hgvsp: ENST00000325241.6:c.1473C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1506C>T
  hgvsp: ENST00000446747.2:c.1506C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1473C>T
  hgvsp: ENST00000528372.1:c.1473C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3399C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-837G>A
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3546
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 84
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3825
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3108
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1363
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1862
  bin: 8.25e1
  variant carriers: 0
hgvs: p.His491His
num of homozygotes: 0
population: African
population: South Asian
population: Latino
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: VQSLOD
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum

8-146067967-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067967
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067967
    reference: chr 8
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1475C>G
  hgvsp: ENSP00000320627.6:p.Thr492Ser
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3397C>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3397C>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-839G>C
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1508C>G
  hgvsp: ENSP00000393260.2:p.Thr503Ser
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5003C>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1475C>G
  hgvsp: ENSP00000432724.1:p.Thr492Ser
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1187C>G
  hgvsp: ENSP00000439424.1:p.Thr396Ser
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3828
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 82
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3105
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3545
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 9.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43190
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 2171
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2031
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Thr492Ser
num of homozygotes: 0
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: C
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: ClippingRankSum

8-146067975-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067975
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067975
    reference: chr 8
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3389A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1195A>G
  hgvsp: ENSP00000439424.1:p.Lys399Glu
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1483A>G
  hgvsp: ENSP00000432724.1:p.Lys495Glu
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-847T>C
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3389A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1483A>G
  hgvsp: ENSP00000320627.6:p.Lys495Glu
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5011A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1516A>G
  hgvsp: ENSP00000393260.2:p.Lys506Glu
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3111
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 731
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3814
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1647
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 20
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 11
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Lys495Glu
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: ReadPosRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

8-146067978-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067978
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067978
    reference: chr 8
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1519C>T
  hgvsp: ENSP00000393260.2:p.Pro507Ser
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3386C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3386C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1486C>T
  hgvsp: ENSP00000432724.1:p.Pro496Ser
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-850G>A
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1486C>T
  hgvsp: ENSP00000320627.6:p.Pro496Ser
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1198C>T
  hgvsp: ENSP00000439424.1:p.Pro400Ser
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5014C>T
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 79
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5886
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3811
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43191
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6630
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1577
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Pro496Ser
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: Latino
population: Other
reference allele: C
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: FS
site quality: MQ
site quality: MQRankSum
site quality: DP
site quality: BaseQRankSum
site quality: ClippingRankSum

8-146067981-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067981
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067981
    reference: chr 8
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-853A>C
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1522T>G
  hgvsp: ENSP00000393260.2:p.Tyr508Asp
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5017T>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3383T>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1201T>G
  hgvsp: ENSP00000439424.1:p.Tyr401Asp
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1489T>G
  hgvsp: ENSP00000432724.1:p.Tyr497Asp
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3383T>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1489T>G
  hgvsp: ENSP00000320627.6:p.Tyr497Asp
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3820
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3547
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 89
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3117
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1647
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1576
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
hgvs: p.Tyr497Asp
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: African
population: European (Non-Finnish)
population: Latino
population: South Asian
population: Other
reference allele: T
site quality: FS
site quality: MQ
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

8-146067982-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067982
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067982
    reference: chr 8
allele count: 2
allele frequency: 1.647772211969417e-5
allele num: 121376
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3382A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3382A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-854T>C
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5018A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1523A>G
  hgvsp: ENSP00000393260.2:p.Tyr508Cys
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1490A>G
  hgvsp: ENSP00000432724.1:p.Tyr497Cys
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1490A>G
  hgvsp: ENSP00000320627.6:p.Tyr497Cys
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1202A>G
  hgvsp: ENSP00000439424.1:p.Tyr401Cys
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1434
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 75
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3816
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3113
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3550
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6609
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1576
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1368
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 21
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2024
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Tyr497Cys
num of homozygotes: 0
population: European (Finnish)
population: European (Non-Finnish)
population: African
population: South Asian
population: East Asian
population: Latino
population: Other
reference allele: A
site quality: FS
site quality: InbreedingCoeff
site quality: MQ
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum
site quality: DP

8-146067986-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067986
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067986
    reference: chr 8
allele count: 3
allele frequency: 2.471658317954126e-5
allele num: 121376
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3378G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5022G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1494G>A
  hgvsp: ENST00000528372.1:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3378G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1527G>A
  hgvsp: ENST00000446747.2:c.1527G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1494G>A
  hgvsp: ENST00000325241.6:c.1494G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1206G>A
  hgvsp: ENST00000544249.1:c.1206G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-858C>T
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 6.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1643
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Val498Val
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: African
population: Other
reference allele: G
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: QD
site quality: VQSLOD

8-146067986-G-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067986
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067986
    reference: chr 8
allele count: 1
allele frequency: 8.238861059847087e-6
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3378G>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-858C>A
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1527G>T
  hgvsp: ENST00000446747.2:c.1527G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3378G>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1494G>T
  hgvsp: ENST00000325241.6:c.1494G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1494G>T
  hgvsp: ENST00000528372.1:c.1494G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5022G>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1206G>T
  hgvsp: ENST00000544249.1:c.1206G>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3112
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5122
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4288
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3810
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 74
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 16
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1643
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Val498Val
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: G
site quality: FS
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: DP
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum

8-146067988-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067988
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067988
    reference: chr 8
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3376G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1496G>A
  hgvsp: ENSP00000432724.1:p.Cys499Tyr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1208G>A
  hgvsp: ENSP00000439424.1:p.Cys403Tyr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1529G>A
  hgvsp: ENSP00000393260.2:p.Cys510Tyr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5024G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3376G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1496G>A
  hgvsp: ENSP00000320627.6:p.Cys499Tyr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-860C>T
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 73
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1930
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1641
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1576
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Cys499Tyr
num of homozygotes: 0
population: East Asian
population: African
population: Latino
population: European (Finnish)
population: South Asian
population: European (Non-Finnish)
population: Other
reference allele: G
site quality: FS
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: QD

8-146067993-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067993
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067993
    reference: chr 8
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3371G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1213G>A
  hgvsp: ENSP00000439424.1:p.Asp405Asn
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1534G>A
  hgvsp: ENSP00000393260.2:p.Asp512Asn
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3371G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1501G>A
  hgvsp: ENSP00000432724.1:p.Asp501Asn
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1501G>A
  hgvsp: ENSP00000320627.6:p.Asp501Asn
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5029G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-865C>T
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 91
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5884
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3115
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3800
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2028
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1868
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Asp501Asn
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: East Asian
population: European (Finnish)
population: Latino
population: Other
population: South Asian
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: ReadPosRankSum
site quality: MQ
site quality: FS
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: BaseQRankSum
site quality: InbreedingCoeff

8-146067999-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146067999
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146067999
    reference: chr 8
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1219G>A
  hgvsp: ENSP00000439424.1:p.Gly407Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-871C>T
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1507G>A
  hgvsp: ENSP00000432724.1:p.Gly503Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5035G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3365G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1540G>A
  hgvsp: ENSP00000393260.2:p.Gly514Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1507G>A
  hgvsp: ENSP00000320627.6:p.Gly503Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3365G>A
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3565
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2056
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7148
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1866
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Gly503Arg
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: African
population: Other
population: European (Non-Finnish)
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD

8-146068004-AGC-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068004
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068002
    reference: chr 8
allele count: 1
allele frequency: 8.238589553468446e-6
allele num: 121380
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-878_*117-877delGC
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3359_281-3358delGC
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1546_1547delGC
  hgvsp: ENSP00000393260.2:p.Ala516LeufsTer15
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3359_248-3358delGC
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1513_1514delGC
  hgvsp: ENSP00000320627.6:p.Ala505LeufsTer15
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1225_1226delGC
  hgvsp: ENSP00000439424.1:p.Ala409LeufsTer15
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1513_1514delGC
  hgvsp: ENSP00000432724.1:p.Ala505LeufsTer15
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5041_5042delGC
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: frameshift
filter: VQSRTrancheINDEL95.00to96.00
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3809
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 94
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2057
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4287
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6975
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1931
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1435
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6375
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1577
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 34
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6642
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ala505LeufsTer15
num of homozygotes: 0
population: Other
population: African
population: South Asian
population: European (Non-Finnish)
population: European (Finnish)
population: Latino
population: East Asian
reference allele: AGC
site quality: QD
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: DP
site quality: InbreedingCoeff
site quality: FS
site quality: MQRankSum
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-146068005-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068005
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068005
    reference: chr 8
allele count: 15
allele frequency: 1.235808795663135e-4
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1513G>A
  hgvsp: ENSP00000320627.6:p.Ala505Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3359G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1513G>A
  hgvsp: ENSP00000432724.1:p.Ala505Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1225G>A
  hgvsp: ENSP00000439424.1:p.Ala409Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1546G>A
  hgvsp: ENSP00000393260.2:p.Ala516Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5041G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-877C>T
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3359G>A
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 733
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4284
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7149
  bin: 5.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3104
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 6.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 2058
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6976
  bin: 4.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 3804
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 992
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 8.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 5881
  bin: 4.25e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2027
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Ala505Thr
num of homozygotes: 0
population: Latino
population: African
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: East Asian
population: South Asian
reference allele: G
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: DP
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: QD

8-146068006-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068006
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068006
    reference: chr 8
allele count: 2
allele frequency: 1.647717910693689e-5
allele num: 121380
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1226C>G
  hgvsp: ENSP00000439424.1:p.Ala409Gly
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1514C>G
  hgvsp: ENSP00000432724.1:p.Ala505Gly
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3358C>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1547C>G
  hgvsp: ENSP00000393260.2:p.Ala516Gly
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3358C>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1514C>G
  hgvsp: ENSP00000320627.6:p.Ala505Gly
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5042C>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-878G>C
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1932
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4285
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6973
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3806
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5121
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2059
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6373
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3107
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1642
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
hgvs: p.Ala505Gly
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: Other
population: East Asian
population: European (Non-Finnish)
reference allele: C
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: FS
site quality: QD
site quality: DP

8-146068015-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068015
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068015
    reference: chr 8
allele count: 1
allele frequency: 8.238318064983852e-6
allele num: 121384
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1556A>G
  hgvsp: ENSP00000393260.2:p.Gln519Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1523A>G
  hgvsp: ENSP00000432724.1:p.Gln508Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1523A>G
  hgvsp: ENSP00000320627.6:p.Gln508Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-887T>C
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3349A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1235A>G
  hgvsp: ENSP00000439424.1:p.Gln412Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5051A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3349A>G
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2060
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3563
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4286
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1436
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6972
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6374
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3807
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3114
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 31
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 10
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1365
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1577
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 2.75e1
  variant carriers: 0
hgvs: p.Gln508Arg
num of homozygotes: 0
population: African
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: European (Finnish)
population: Other
population: Latino
reference allele: A
site quality: DP
site quality: FS
site quality: ReadPosRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: QD
site quality: ClippingRankSum

8-146068022-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068022
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068022
    reference: chr 8
allele count: 4
allele frequency: 3.295544423938835e-5
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1242C>T
  hgvsp: ENST00000544249.1:c.1242C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-894G>A
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1563C>T
  hgvsp: ENST00000446747.2:c.1563C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3342C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5058C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1530C>T
  hgvsp: ENST00000325241.6:c.1530C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1530C>T
  hgvsp: ENST00000528372.1:c.1530C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3342C>T
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3794
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 81
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3569
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6971
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6376
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 71
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5885
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 7.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6612
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1366
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43205
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2026
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Ser510Ser
num of homozygotes: 0
population: South Asian
population: Other
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: East Asian
population: Latino
reference allele: C
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: MQ
site quality: VQSLOD
site quality: MQRankSum
site quality: FS
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: ReadPosRankSum

http://identifiers.org/exac.variant/8-146068029-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068029
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068029
    reference: chr 8
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1249A>C
  hgvsp: ENSP00000439424.1:p.Ile417Leu
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1570A>C
  hgvsp: ENSP00000393260.2:p.Ile524Leu
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1537A>C
  hgvsp: ENSP00000320627.6:p.Ile513Leu
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-901T>G
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5065A>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3335A>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1537A>C
  hgvsp: ENSP00000432724.1:p.Ile513Leu
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3335A>C
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4283
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 93
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7150
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5120
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2170
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1579
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Ile513Leu
num of homozygotes: 0
population: East Asian
population: African
population: European (Finnish)
population: Other
population: South Asian
population: European (Non-Finnish)
population: Latino
reference allele: A
site quality: VQSLOD
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: ClippingRankSum
site quality: ReadPosRankSum
site quality: MQRankSum

8-146068030-TTTAC-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068030
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068026
    reference: chr 8
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1539_1542delTTAC
  hgvsp: ENSP00000432724.1:p.Tyr514IlefsTer22
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1539_1542delTTAC
  hgvsp: ENSP00000320627.6:p.Tyr514IlefsTer22
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1251_1254delTTAC
  hgvsp: ENSP00000439424.1:p.Tyr418IlefsTer22
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1572_1575delTTAC
  hgvsp: ENSP00000393260.2:p.Tyr525IlefsTer22
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-906_*117-903delGTAA
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5067_5070delTTAC
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3333_281-3330delTTAC
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3333_248-3330delTTAC
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 993
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7151
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 92
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3996
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1933
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4282
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3791
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5882
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5119
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3557
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1368
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Tyr514IlefsTer22
num of homozygotes: 0
population: South Asian
population: East Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: Other
reference allele: TTTAC
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: BaseQRankSum
site quality: MQ
site quality: ClippingRankSum
site quality: VQSLOD
site quality: QD
site quality: FS
site quality: DP
site quality: ReadPosRankSum

8-146068049-T-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068049
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068049
    reference: chr 8
allele count: 2
allele frequency: 1.64774506088418e-5
allele num: 121378
alternate allele: C
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1557T>C
  hgvsp: ENST00000528372.1:c.1557T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1557T>C
  hgvsp: ENST00000325241.6:c.1557T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1269T>C
  hgvsp: ENST00000544249.1:c.1269T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1590T>C
  hgvsp: ENST00000446747.2:c.1590T>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3315T>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3315T>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5085T>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-921A>G
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 8.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3576
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 80
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6970
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2063
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43212
  bin: 9.75e1
  variant carriers: 2
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2173
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1636
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1871
  bin: 8.25e1
  variant carriers: 0
hgvs: p.His519His
num of homozygotes: 0
population: East Asian
population: Latino
population: European (Non-Finnish)
population: Other
population: European (Finnish)
population: African
population: South Asian
reference allele: T
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: BaseQRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: MQ
site quality: FS
site quality: ReadPosRankSum
site quality: QD

8-146068058-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068058
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068058
    reference: chr 8
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1278G>A
  hgvsp: ENST00000544249.1:c.1278G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5094G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1599G>A
  hgvsp: ENST00000446747.2:c.1599G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3306G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1566G>A
  hgvsp: ENST00000325241.6:c.1566G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3306G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1566G>A
  hgvsp: ENST00000528372.1:c.1566G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-930C>T
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3577
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3132
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1437
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5118
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3790
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6971
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 995
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1364
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 27
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43215
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Glu522Glu
num of homozygotes: 0
population: Other
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: East Asian
population: African
population: South Asian
reference allele: G
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: DP

8-146068060-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068060
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068060
    reference: chr 8
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-932T>C
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1601A>G
  hgvsp: ENSP00000393260.2:p.Lys534Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1568A>G
  hgvsp: ENSP00000432724.1:p.Lys523Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5096A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1568A>G
  hgvsp: ENSP00000320627.6:p.Lys523Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3304A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1280A>G
  hgvsp: ENSP00000439424.1:p.Lys427Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3304A>G
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 732
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3580
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5117
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3995
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1438
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3133
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 68
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 66
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6969
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6377
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2062
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7153
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4280
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3789
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5883
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1934
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 994
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1640
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43215
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 45
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 6.75e1
  variant carriers: 0
hgvs: p.Lys523Arg
num of homozygotes: 0
population: Other
population: South Asian
population: European (Finnish)
population: African
population: Latino
population: European (Non-Finnish)
population: East Asian
reference allele: A
site quality: QD
site quality: MQRankSum
site quality: ClippingRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: MQ
site quality: FS
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

8-146068067-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068067
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068067
    reference: chr 8
allele count: 240
allele frequency: 1.977326654363301e-3
allele num: 121376
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1575C>T
  hgvsp: ENST00000325241.6:c.1575C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3297C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1575C>T
  hgvsp: ENST00000528372.1:c.1575C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1287C>T
  hgvsp: ENST00000544249.1:c.1287C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-939G>A
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3297C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1608C>T
  hgvsp: ENST00000446747.2:c.1608C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5103C>T
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 2.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 6.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 3.75e1
  variant carriers: 6
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 6.25e1
  variant carriers: 12
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 9.75e1
  variant carriers: 97
genotype depth: GenotypeDepth
  all individuals: 3762
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1449
  bin: 8.25e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 3121
  bin: 3.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 5.25e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 5866
  bin: 4.25e1
  variant carriers: 8
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 9.25e1
  variant carriers: 13
genotype depth: GenotypeDepth
  all individuals: 1007
  bin: 8.75e1
  variant carriers: 14
genotype depth: GenotypeDepth
  all individuals: 2078
  bin: 7.75e1
  variant carriers: 20
genotype depth: GenotypeDepth
  all individuals: 6366
  bin: 5.75e1
  variant carriers: 7
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 4.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3127
  bin: 7.25e1
  variant carriers: 13
genotype quality: GenotypeQuality
  all individuals: 2034
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1861
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1633
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 42
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Tyr525Tyr
num of homozygotes: 4
population: Other
population: East Asian
population: European (Non-Finnish)
population: European (Finnish)
population: African
population: South Asian
population: Latino
reference allele: C
site quality: MQRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: BaseQRankSum
site quality: FS
site quality: VQSLOD
site quality: QD
site quality: InbreedingCoeff
site quality: DP
site quality: ReadPosRankSum

8-146068068-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068068
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068068
    reference: chr 8
allele count: 1
allele frequency: 8.2387253044209e-6
allele num: 121378
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1288G>A
  hgvsp: ENSP00000439424.1:p.Glu430Lys
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-940C>T
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1576G>A
  hgvsp: ENSP00000432724.1:p.Glu526Lys
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3296G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5104G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1609G>A
  hgvsp: ENSP00000393260.2:p.Glu537Lys
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1576G>A
  hgvsp: ENSP00000320627.6:p.Glu526Lys
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3296G>A
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 63
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3766
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 60
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3581
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6367
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 13
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2011
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4270
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 735
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1634
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 19
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43271
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Glu526Lys
num of homozygotes: 0
population: East Asian
population: Other
population: African
population: European (Finnish)
population: South Asian
population: Latino
population: European (Non-Finnish)
reference allele: G
site quality: MQ
site quality: ClippingRankSum
site quality: DP
site quality: MQRankSum
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: QD

8-146068074-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068074
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068074
    reference: chr 8
allele count: 1
allele frequency: 8.238453806989504e-6
allele num: 121382
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1294C>T
  hgvsp: ENSP00000439424.1:p.Leu432Phe
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1615C>T
  hgvsp: ENSP00000393260.2:p.Leu539Phe
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5110C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1582C>T
  hgvsp: ENSP00000320627.6:p.Leu528Phe
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3290C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3290C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1582C>T
  hgvsp: ENSP00000432724.1:p.Leu528Phe
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-946G>A
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 14
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3588
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6954
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6367
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2012
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5870
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2166
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 14
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1867
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 37
  bin: 2.25e1
  variant carriers: 0
hgvs: p.Leu528Phe
num of homozygotes: 0
population: East Asian
population: Other
population: Latino
population: African
population: European (Finnish)
population: European (Non-Finnish)
population: South Asian
reference allele: C
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: BaseQRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: QD
site quality: ClippingRankSum

8-146068079-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068079
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068079
    reference: chr 8
allele count: 4
allele frequency: 3.29549012176836e-5
allele num: 121378
alternate allele: G
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1587A>G
  hgvsp: ENST00000528372.1:c.1587A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1299A>G
  hgvsp: ENST00000544249.1:c.1299A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1587A>G
  hgvsp: ENST00000325241.6:c.1587A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5115A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3285A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1620A>G
  hgvsp: ENST00000446747.2:c.1620A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3285A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-951T>C
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3756
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5112
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 15
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6366
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1001
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 736
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6952
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2016
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 12
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43272
  bin: 9.75e1
  variant carriers: 4
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2164
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Gln529Gln
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: African
population: East Asian
population: Other
population: South Asian
reference allele: A
site quality: DP
site quality: BaseQRankSum
site quality: MQRankSum
site quality: MQ
site quality: InbreedingCoeff
site quality: QD
site quality: FS
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: VQSLOD

8-146068082-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068082
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068082
    reference: chr 8
allele count: 15
allele frequency: 1.235910618944038e-4
allele num: 121368
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1590C>T
  hgvsp: ENST00000325241.6:c.1590C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1302C>T
  hgvsp: ENST00000544249.1:c.1302C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1590C>T
  hgvsp: ENST00000528372.1:c.1590C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5118C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3282C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-954G>A
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1623C>T
  hgvsp: ENST00000446747.2:c.1623C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3282C>T
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2021
  bin: 9.75e1
  variant carriers: 9
genotype depth: GenotypeDepth
  all individuals: 3992
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3584
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 739
  bin: 9.25e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 1000
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3754
  bin: 2.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3126
  bin: 3.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 17
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 65
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6953
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 7.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 25
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1352
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1631
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Cys530Cys
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: African
population: European (Finnish)
population: Other
reference allele: C
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: DP
site quality: QD
site quality: InbreedingCoeff
site quality: VQSLOD
site quality: FS
site quality: MQ

8-146068083-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068083
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068083
    reference: chr 8
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: A
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1591G>A
  hgvsp: ENSP00000432724.1:p.Gly531Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-955C>T
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3281G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1591G>A
  hgvsp: ENSP00000320627.6:p.Gly531Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1303G>A
  hgvsp: ENSP00000439424.1:p.Gly435Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1624G>A
  hgvsp: ENSP00000393260.2:p.Gly542Arg
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3281G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5119G>A
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 7135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3753
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3586
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 62
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 23
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 30
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 18
  bin: 4.25e1
  variant carriers: 0
hgvs: p.Gly531Arg
num of homozygotes: 0
population: East Asian
population: European (Finnish)
population: South Asian
population: Latino
population: Other
population: African
population: European (Non-Finnish)
reference allele: G
site quality: DP
site quality: VQSLOD
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: FS
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

8-146068086-A-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068086
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068086
    reference: chr 8
allele count: 1
allele frequency: 8.239268352970255e-6
allele num: 121370
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3278A>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: stop_gained
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1594A>T
  hgvsp: ENSP00000432724.1:p.Lys532Ter
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5122A>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-958T>A
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3278A>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1306A>T
  hgvsp: ENSP00000439424.1:p.Lys436Ter
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1594A>T
  hgvsp: ENSP00000320627.6:p.Lys532Ter
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: stop_gained
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1627A>T
  hgvsp: ENSP00000393260.2:p.Lys543Ter
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: stop gained
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 61
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 16
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 67
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3589
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3750
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2018
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3125
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 7
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 17
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43275
  bin: 9.75e1
  variant carriers: 1
genotype quality: GenotypeQuality
  all individuals: 6617
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2041
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1630
  bin: 7.75e1
  variant carriers: 0
hgvs: p.Lys532Ter
num of homozygotes: 0
population: European (Non-Finnish)
population: Other
population: East Asian
population: South Asian
population: Latino
population: African
population: European (Finnish)
reference allele: A
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: FS
site quality: QD
site quality: ReadPosRankSum
site quality: ClippingRankSum
site quality: MQ
site quality: MQRankSum
site quality: DP

8-146068090-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068090
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068090
    reference: chr 8
allele count: 2
allele frequency: 1.647935137272997e-5
allele num: 121364
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3274C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5126C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1310C>T
  hgvsp: ENSP00000439424.1:p.Ala437Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1598C>T
  hgvsp: ENSP00000320627.6:p.Ala533Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3274C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1598C>T
  hgvsp: ENSP00000432724.1:p.Ala533Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1631C>T
  hgvsp: ENSP00000393260.2:p.Ala544Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-962G>A
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 64
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 18
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3579
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2019
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7137
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3746
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 69
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1582
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 15
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6599
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 46
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2165
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 32
  bin: 3.25e1
  variant carriers: 0
hgvs: p.Ala533Val
num of homozygotes: 0
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: C
site quality: VQSLOD
site quality: FS
site quality: ReadPosRankSum
site quality: MQRankSum
site quality: MQ
site quality: DP
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: BaseQRankSum

8-146068102-G-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068102
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068102
    reference: chr 8
allele count: 13
allele frequency: 1.071157839227448e-4
allele num: 121364
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3262G>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1643G>C
  hgvsp: ENSP00000393260.2:p.Ser548Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1610G>C
  hgvsp: ENSP00000432724.1:p.Ser537Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5138G>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1322G>C
  hgvsp: ENSP00000439424.1:p.Ser441Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1610G>C
  hgvsp: ENSP00000320627.6:p.Ser537Thr
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3262G>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-974C>G
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2022
  bin: 9.75e1
  variant carriers: 4
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 5.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 3.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5111
  bin: 6.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3728
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 78
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 8.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 90
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6949
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5865
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2028
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 28
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Ser537Thr
num of homozygotes: 1
population: Latino
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: European (Finnish)
population: South Asian
reference allele: G
site quality: MQ
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: MQRankSum
site quality: QD

8-146068104-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068104
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068104
    reference: chr 8
allele count: 1
allele frequency: 8.239132584121543e-6
allele num: 121372
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1612A>G
  hgvsp: ENSP00000320627.6:p.Thr538Ala
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1645A>G
  hgvsp: ENSP00000393260.2:p.Thr549Ala
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5140A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3260A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1612A>G
  hgvsp: ENSP00000432724.1:p.Thr538Ala
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-976T>C
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1324A>G
  hgvsp: ENSP00000439424.1:p.Thr442Ala
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3260A>G
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3552
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3723
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5867
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3135
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 19
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 83
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6950
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4271
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 96
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7136
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 24
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1634
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 35
  bin: 5.75e1
  variant carriers: 0
hgvs: p.Thr538Ala
num of homozygotes: 0
population: European (Finnish)
population: Latino
population: East Asian
population: South Asian
population: African
population: European (Non-Finnish)
population: Other
reference allele: A
site quality: BaseQRankSum
site quality: ClippingRankSum
site quality: MQRankSum
site quality: MQ
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: FS
site quality: DP
site quality: QD

8-146068110-C-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068110
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068110
    reference: chr 8
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3254C>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-982G>C
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3254C>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1618C>G
  hgvsp: ENSP00000432724.1:p.Leu540Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1651C>G
  hgvsp: ENSP00000393260.2:p.Leu551Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1618C>G
  hgvsp: ENSP00000320627.6:p.Leu540Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1330C>G
  hgvsp: ENSP00000439424.1:p.Leu444Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5146C>G
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6952
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1638
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu540Val
num of homozygotes: 0
population: South Asian
population: Other
population: African
population: East Asian
population: Latino
population: European (Non-Finnish)
population: European (Finnish)
reference allele: C
site quality: DP
site quality: ClippingRankSum
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: QD

8-146068110-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068110
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068110
    reference: chr 8
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: T
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1651C>T
  hgvsp: ENSP00000393260.2:p.Leu551Phe
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1618C>T
  hgvsp: ENSP00000320627.6:p.Leu540Phe
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1618C>T
  hgvsp: ENSP00000432724.1:p.Leu540Phe
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-982G>A
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1330C>T
  hgvsp: ENSP00000439424.1:p.Leu444Phe
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3254C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3254C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5146C>T
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3555
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4275
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6952
  bin: 4.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3715
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7135
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 85
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5871
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2073
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2023
  bin: 9.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 737
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6524
  bin: 6.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 13
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1584
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Leu540Phe
num of homozygotes: 0
population: South Asian
population: European (Finnish)
population: Latino
population: European (Non-Finnish)
population: Other
population: African
population: East Asian
reference allele: C
site quality: MQ
site quality: BaseQRankSum
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: QD
site quality: ClippingRankSum
site quality: FS
site quality: VQSLOD
site quality: DP

http://identifiers.org/exac.variant/8-146068115-A-C
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068115
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068115
    reference: chr 8
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: C
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1656A>C
  hgvsp: ENST00000446747.2:c.1656A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-987T>G
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3249A>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5151A>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1623A>C
  hgvsp: ENST00000325241.6:c.1623A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3249A>C
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1623A>C
  hgvsp: ENST00000528372.1:c.1623A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1335A>C
  hgvsp: ENST00000544249.1:c.1335A>C(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1353
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 3
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2163
  bin: 9.25e1
  variant carriers: 0
hgvs: p.Thr541Thr
num of homozygotes: 0
population: African
population: European (Non-Finnish)
population: East Asian
population: Other
population: South Asian
population: Latino
population: European (Finnish)
reference allele: A
site quality: BaseQRankSum
site quality: QD
site quality: MQ
site quality: VQSLOD
site quality: FS
site quality: ClippingRankSum
site quality: DP
site quality: InbreedingCoeff
site quality: ReadPosRankSum
site quality: MQRankSum

8-146068115-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068115
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068115
    reference: chr 8
allele count: 1
allele frequency: 8.239539904091756e-6
allele num: 121366
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-987T>C
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1335A>G
  hgvsp: ENST00000544249.1:c.1335A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1656A>G
  hgvsp: ENST00000446747.2:c.1656A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1623A>G
  hgvsp: ENST00000325241.6:c.1623A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3249A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1623A>G
  hgvsp: ENST00000528372.1:c.1623A>G(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3249A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5151A>G
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2039
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1863
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 40
  bin: 3.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1637
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
hgvs: p.Thr541Thr
num of homozygotes: 0
population: European (Non-Finnish)
population: Latino
population: European (Finnish)
population: African
population: Other
population: South Asian
population: East Asian
reference allele: A
site quality: QD
site quality: VQSLOD
site quality: FS
site quality: MQ
site quality: BaseQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: ClippingRankSum
site quality: MQRankSum
site quality: ReadPosRankSum

8-146068115-AAT-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068115
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068113
    reference: chr 8
allele count: 3
allele frequency: 2.471861971227527e-5
allele num: 121366
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-989_*117-988delAT
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: true
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1625_1626delTA
  hgvsp: ENSP00000432724.1:p.Ile542ThrfsTer12
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1625_1626delTA
  hgvsp: ENSP00000320627.6:p.Ile542ThrfsTer12
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3247_248-3246delTA
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1337_1338delTA
  hgvsp: ENSP00000439424.1:p.Ile446ThrfsTer12
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5153_5154delTA
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3247_281-3246delTA
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: frameshift_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1658_1659delTA
  hgvsp: ENSP00000393260.2:p.Ile553ThrfsTer12
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: frameshift
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 86
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3119
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4276
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3706
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5868
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3559
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 111
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 59
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 38
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 22
  bin: 5.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 6498
  bin: 6.25e1
  variant carriers: 0
hgvs: p.Ile542ThrfsTer12
num of homozygotes: 0
population: European (Non-Finnish)
population: African
population: Latino
population: South Asian
population: European (Finnish)
population: East Asian
population: Other
reference allele: AAT
site quality: InbreedingCoeff
site quality: DP
site quality: BaseQRankSum
site quality: FS
site quality: ClippingRankSum
site quality: MQRankSum
site quality: QD
site quality: VQSLOD
site quality: ReadPosRankSum
site quality: MQ

8-146068116-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068116
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068116
    reference: chr 8
allele count: 4
allele frequency: 3.295924589245398e-5
allele num: 121362
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1657A>G
  hgvsp: ENSP00000393260.2:p.Ile553Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1624A>G
  hgvsp: ENSP00000320627.6:p.Ile542Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3248A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1624A>G
  hgvsp: ENSP00000432724.1:p.Ile542Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-988T>C
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1336A>G
  hgvsp: ENSP00000439424.1:p.Ile446Val
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5152A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3248A>G
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3704
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5110
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3561
  bin: 2.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 87
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3120
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 109
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4273
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1002
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7134
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 9.75e1
  variant carriers: 3
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6363
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5869
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1450
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1583
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 26
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 60
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 39
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Ile542Val
num of homozygotes: 0
population: Latino
population: Other
population: European (Non-Finnish)
population: African
population: East Asian
population: South Asian
population: European (Finnish)
reference allele: A
site quality: MQRankSum
site quality: ClippingRankSum
site quality: FS
site quality: DP
site quality: ReadPosRankSum
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: BaseQRankSum
site quality: MQ
site quality: QD

8-146068127-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068127
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068127
    reference: chr 8
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1635G>A
  hgvsp: ENST00000325241.6:c.1635G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1668G>A
  hgvsp: ENST00000446747.2:c.1668G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1635G>A
  hgvsp: ENST00000528372.1:c.1635G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5163G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1347G>A
  hgvsp: ENST00000544249.1:c.1347G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3237G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3237G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-999C>T
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 118
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 98
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3692
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1003
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 21
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3538
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6952
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4274
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5109
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3129
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3123
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2168
  bin: 9.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 36
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.75e1
  variant carriers: 0
hgvs: p.Arg545Arg
num of homozygotes: 0
population: Other
population: South Asian
population: African
population: Latino
population: East Asian
population: European (Finnish)
population: European (Non-Finnish)
reference allele: G
site quality: VQSLOD
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: DP
site quality: MQ
site quality: ClippingRankSum
site quality: QD
site quality: FS
site quality: BaseQRankSum
site quality: ReadPosRankSum

8-146068134-A-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068134
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068134
    reference: chr 8
allele count: 1
allele frequency: 8.239404126293587e-6
allele num: 121368
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5170A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-1006T>C
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1675A>G
  hgvsp: ENSP00000393260.2:p.Thr559Ala
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3230A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3230A>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1642A>G
  hgvsp: ENSP00000320627.6:p.Thr548Ala
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1354A>G
  hgvsp: ENSP00000439424.1:p.Thr452Ala
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1642A>G
  hgvsp: ENSP00000432724.1:p.Thr548Ala
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3553
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5873
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2072
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3683
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2025
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3128
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 115
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 100
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4272
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1642
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 61
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 29
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1354
  bin: 7.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 1.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 43
  bin: 3.75e1
  variant carriers: 0
hgvs: p.Thr548Ala
num of homozygotes: 0
population: European (Finnish)
population: African
population: South Asian
population: European (Non-Finnish)
population: East Asian
population: Other
population: Latino
reference allele: A
site quality: ReadPosRankSum
site quality: BaseQRankSum
site quality: FS
site quality: DP
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: MQRankSum
site quality: MQ
site quality: QD
site quality: ClippingRankSum

8-146068145-G-A
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068145
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068145
    reference: chr 8
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: A
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-1017C>T
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1653G>A
  hgvsp: ENST00000528372.1:c.1653G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3219G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5181G>A
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1365G>A
  hgvsp: ENST00000544249.1:c.1365G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1686G>A
  hgvsp: ENST00000446747.2:c.1686G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1653G>A
  hgvsp: ENST00000325241.6:c.1653G>A(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3219G>A
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3570
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5108
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 8.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5875
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 20
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2026
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 125
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3994
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6952
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7133
  bin: 5.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1
  bin: 7.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 44
  bin: 4.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 4.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 4
  bin: 1.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1356
  bin: 7.25e1
  variant carriers: 0
hgvs: p.Arg551Arg
num of homozygotes: 0
population: East Asian
population: European (Non-Finnish)
population: South Asian
population: Latino
population: European (Finnish)
population: African
population: Other
reference allele: G
site quality: MQRankSum
site quality: QD
site quality: BaseQRankSum
site quality: MQ
site quality: VQSLOD
site quality: InbreedingCoeff
site quality: DP
site quality: FS
site quality: ClippingRankSum
site quality: ReadPosRankSum

8-146068148-C-T
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068148
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068148
    reference: chr 8
allele count: 2
allele frequency: 1.647989452867502e-5
allele num: 121360
alternate allele: T
annotation: Annotation
  canonical: true
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1656C>T
  hgvsp: ENST00000528372.1:c.1656C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3216C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-1020G>A
  variant of: http://identifiers.org/hgnc/17902
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5184C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3216C>T
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1689C>T
  hgvsp: ENST00000446747.2:c.1689C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1368C>T
  hgvsp: ENST00000544249.1:c.1368C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: synonymous_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1656C>T
  hgvsp: ENST00000325241.6:c.1656C>T(p.%3D)
  variant of: http://identifiers.org/hgnc/13139
canonical: true
consequence: synonymous
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 3122
  bin: 7.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5107
  bin: 6.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2028
  bin: 9.75e1
  variant carriers: 2
genotype depth: GenotypeDepth
  all individuals: 6952
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5876
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3653
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3131
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3567
  bin: 2.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1451
  bin: 8.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 41
  bin: 3.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 2035
  bin: 6.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1643
  bin: 7.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 72
  bin: 2.25e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 33
  bin: 2.75e1
  variant carriers: 0
genotype quality: GenotypeQuality
  all individuals: 1865
  bin: 8.25e1
  variant carriers: 0
hgvs: p.Pro552Pro
num of homozygotes: 0
population: Latino
population: South Asian
population: East Asian
population: Other
population: European (Non-Finnish)
population: African
population: European (Finnish)
reference allele: C
site quality: DP
site quality: MQRankSum
site quality: InbreedingCoeff
site quality: ClippingRankSum
site quality: QD
site quality: MQ
site quality: BaseQRankSum
site quality: ReadPosRankSum
site quality: FS
site quality: VQSLOD

8-146068149-T-G
type: Variant
location: Region
  begin: Position
    type: ExactPosition
    position: 146068149
    reference: chr 8
  end: Position
    type: ExactPosition
    position: 146068149
    reference: chr 8
allele count: 1
allele frequency: 8.240083060037246e-6
allele num: 121358
alternate allele: G
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000393260
  ensembl transcript: ENST00000446747
  gene symbol: ZNF7
  hgvsc: ENST00000446747.2:c.1690T>G
  hgvsp: ENSP00000393260.2:p.Tyr564Asp
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: true
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000432724
  ensembl transcript: ENST00000528372
  gene symbol: ZNF7
  hgvsc: ENST00000528372.1:c.1657T>G
  hgvsp: ENSP00000432724.1:p.Tyr553Asp
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000435252
  ensembl transcript: ENST00000525266
  gene symbol: ZNF7
  hgvsc: ENST00000525266.1:c.248-3215T>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000439424
  ensembl transcript: ENST00000544249
  gene symbol: ZNF7
  hgvsc: ENST00000544249.1:c.1369T>G
  hgvsp: ENSP00000439424.1:p.Tyr457Asp
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: missense_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000320627
  ensembl transcript: ENST00000325241
  gene symbol: ZNF7
  hgvsc: ENST00000325241.6:c.1657T>G
  hgvsp: ENSP00000320627.6:p.Tyr553Asp
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: intron_variant
  ensembl gene: ENSG00000147789
  ensembl protein: ENSP00000318848
  ensembl transcript: ENST00000325217
  gene symbol: ZNF7
  hgvsc: ENST00000325217.5:c.281-3215T>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: non_coding_transcript_variant
  consequence: non_coding_transcript_exon_variant
  ensembl gene: ENSG00000147789
  ensembl transcript: ENST00000528017
  gene symbol: ZNF7
  hgvsc: ENST00000528017.1:n.5185T>G
  variant of: http://identifiers.org/hgnc/13139
annotation: Annotation
  canonical: false
  consequence: NMD_transcript_variant
  consequence: intron_variant
  ensembl gene: ENSG00000170619
  ensembl protein: ENSP00000436382
  ensembl transcript: ENST00000530332
  gene symbol: COMMD5
  hgvsc: ENST00000530332.1:c.*117-1021A>C
  variant of: http://identifiers.org/hgnc/17902
canonical: true
consequence: missense
filter: PASS
genotype depth: GenotypeDepth
  all individuals: 2029
  bin: 9.75e1
  variant carriers: 1
genotype depth: GenotypeDepth
  all individuals: 738
  bin: 9.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6951
  bin: 4.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3130
  bin: 3.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 101
  bin: 1.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 23
  bin: 7.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 5877
  bin: 4.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 0
  bin: 2.5e0
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3993
  bin: 6.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 4269
  bin: 3.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 6364
  bin: 5.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 2071
  bin: 7.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 3659
  bin: 2.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 123
  bin: 1.75e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 7133
  bin: 5.25e1
  variant carriers: 0
genotype depth: GenotypeDepth
  all individuals: 1004
  bin: 8.75e1
  variant carriers: 0
hgvs: p.Tyr553Asp
num of homozygotes: 0
reference allele: T

GenotypeQuality
all individuals: 1604
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1845
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5191
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1150
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1859
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 149
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 122
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43177
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 1312
bin: 7.25e1
variant carriers: 0

African
type: Population
allele count: 1
allele frequency: 1.037559659680432e-4
allele num: 9638
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)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65190
num of homozygotes: 0

South Asian
type: Population
allele count: 1
allele frequency: 6.06134076857801e-5
allele num: 16498
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: 894
num of homozygotes: 0

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

FS
type: SiteQuality
SIO_000300: 3.129e0

MQRankSum
type: SiteQuality
SIO_000300: 1.37e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.0e-1

MQ
type: SiteQuality
SIO_000300: 5.974e1

ClippingRankSum
type: SiteQuality
SIO_000300: -3.65e-1

VQSLOD
type: SiteQuality
SIO_000300: 1.72e0

BaseQRankSum
type: SiteQuality
SIO_000300: 1.33e0

DP
type: SiteQuality
SIO_000300: 3.178056e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-3

QD
type: SiteQuality
SIO_000300: 1.112e1

GenotypeQuality
all individuals: 38
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5238
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 145
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1570
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 117
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 1609
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1145
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2165
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 146
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1858
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 52
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43175
bin: 9.75e1
variant carriers: 1

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.532801961986511e-5
allele num: 65240
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: 8648
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9670
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.974e1

QD
type: SiteQuality
SIO_000300: 1.403e1

VQSLOD
type: SiteQuality
SIO_000300: 1.04e0

MQRankSum
type: SiteQuality
SIO_000300: 1.76e0

FS
type: SiteQuality
SIO_000300: 1.773e0

BaseQRankSum
type: SiteQuality
SIO_000300: -4.665e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.95e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 4.3e-3

DP
type: SiteQuality
SIO_000300: 3.179038e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e0

GenotypeQuality
all individuals: 1879
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 37
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 75
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 47
bin: 4.25e1
variant carriers: 0

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

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

GenotypeQuality
all individuals: 43175
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1315
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 56
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2163
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1613
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1140
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 54
bin: 4.75e1
variant carriers: 0

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

African
type: Population
allele count: 1
allele frequency: 1.029230135858378e-4
allele num: 9716
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 65340
num of homozygotes: 0

South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 16500
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: 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: 6612
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: -6.76e-1

MQRankSum
type: SiteQuality
SIO_000300: -1.219e0

DP
type: SiteQuality
SIO_000300: 3.181233e6

VQSLOD
type: SiteQuality
SIO_000300: -1.633e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.44e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

FS
type: SiteQuality
SIO_000300: 1.0543e1

MQ
type: SiteQuality
SIO_000300: 5.96e1

BaseQRankSum
type: SiteQuality
SIO_000300: -4.94e0

QD
type: SiteQuality
SIO_000300: 1.281e1

GenotypeQuality
all individuals: 1913
bin: 6.75e1
variant carriers: 0

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

GenotypeQuality
all individuals: 5582
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 66
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 12
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 113
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 34
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 991
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43177
bin: 9.75e1
variant carriers: 1

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

GenotypeQuality
all individuals: 17
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1574
bin: 8.75e1
variant carriers: 0

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

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

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

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

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 902
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9828
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 2.18e-1

QD
type: SiteQuality
SIO_000300: 1.046e1

DP
type: SiteQuality
SIO_000300: 3.185954e6

FS
type: SiteQuality
SIO_000300: 4.635e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.0e-3

MQ
type: SiteQuality
SIO_000300: 5.947e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.912e0

BaseQRankSum
type: SiteQuality
SIO_000300: -5.47e-1

VQSLOD
type: SiteQuality
SIO_000300: 4.64e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.75e0

GenotypeQuality
all individuals: 13
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 2
bin: 2.5e0
variant carriers: 0

GenotypeQuality
all individuals: 57
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 866
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 5754
bin: 6.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1624
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 31
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 99
bin: 2.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43178
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 1329
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1574
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1928
bin: 6.75e1
variant carriers: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 9888
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: 902
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: 1
allele frequency: 1.519849230956289e-5
allele num: 65796
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: 8650
num of homozygotes: 0

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.09e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 6.8e-3

FS
type: SiteQuality
SIO_000300: 2.87e0

BaseQRankSum
type: SiteQuality
SIO_000300: 2.06e0

VQSLOD
type: SiteQuality
SIO_000300: 7.04e-1

MQRankSum
type: SiteQuality
SIO_000300: -9.2e-2

MQ
type: SiteQuality
SIO_000300: 5.931e1

QD
type: SiteQuality
SIO_000300: 1.426e1

DP
type: SiteQuality
SIO_000300: 3.188501e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.9e-2

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 49
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43178
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2165
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 38
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1330
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 839
bin: 2.25e1
variant carriers: 0

GenotypeQuality
all individuals: 53
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 10
bin: 7.5e0
variant carriers: 0

GenotypeQuality
all individuals: 26
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 1574
bin: 8.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1844
bin: 8.25e1
variant carriers: 0

GenotypeQuality
all individuals: 103
bin: 3.25e1
variant carriers: 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
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Other
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 1.518971959777622e-5
allele num: 65834
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East Asian
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ReadPosRankSum
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InbreedingCoeff
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BaseQRankSum
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FS
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QD
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DP
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MQRankSum
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MQ
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VQSLOD
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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num of homozygotes: 0

Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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Other
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East Asian
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VQSLOD
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BaseQRankSum
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MQ
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MQRankSum
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InbreedingCoeff
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DP
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ClippingRankSum
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FS
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele frequency: 1.15606936416185e-4
allele num: 8650
num of homozygotes: 0

Latino
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num of homozygotes: 0

Other
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allele frequency: 0.0e0
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European (Finnish)
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele frequency: 0.0e0
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African
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South Asian
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MQ
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BaseQRankSum
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FS
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DP
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VQSLOD
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MQRankSum
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InbreedingCoeff
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QD
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Non-Finnish)
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allele num: 66074
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European (Finnish)
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African
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East Asian
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South Asian
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Latino
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allele frequency: 0.0e0
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Other
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BaseQRankSum
type: SiteQuality
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DP
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MQ
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ClippingRankSum
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MQRankSum
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FS
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VQSLOD
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InbreedingCoeff
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ReadPosRankSum
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

European (Finnish)
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allele frequency: 0.0e0
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Other
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allele frequency: 0.0e0
allele num: 904
num of homozygotes: 0

European (Non-Finnish)
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allele frequency: 1.509479531457553e-5
allele num: 66248
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Latino
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South Asian
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African
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MQ
type: SiteQuality
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ReadPosRankSum
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VQSLOD
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QD
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DP
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BaseQRankSum
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InbreedingCoeff
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MQRankSum
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FS
type: SiteQuality
SIO_000300: 7.77e0

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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Latino
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South Asian
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European (Non-Finnish)
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African
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European (Finnish)
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Other
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East Asian
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InbreedingCoeff
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VQSLOD
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MQRankSum
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ReadPosRankSum
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ClippingRankSum
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QD
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FS
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MQ
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BaseQRankSum
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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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South Asian
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European (Non-Finnish)
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African
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East Asian
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European (Finnish)
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Latino
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Other
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MQRankSum
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DP
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ClippingRankSum
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ReadPosRankSum
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MQ
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VQSLOD
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FS
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InbreedingCoeff
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BaseQRankSum
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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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European (Non-Finnish)
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East Asian
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Latino
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African
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European (Finnish)
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Other
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South Asian
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MQRankSum
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MQ
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ReadPosRankSum
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VQSLOD
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QD
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FS
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BaseQRankSum
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InbreedingCoeff
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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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East Asian
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European (Non-Finnish)
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European (Finnish)
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Latino
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African
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South Asian
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MQ
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ReadPosRankSum
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FS
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MQRankSum
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BaseQRankSum
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VQSLOD
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QD
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ClippingRankSum
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DP
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66626
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

South Asian
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allele count: 1
allele frequency: 6.059871530723549e-5
allele num: 16502
num of homozygotes: 0

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

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

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.06e0

FS
type: SiteQuality
SIO_000300: 6.049e0

QD
type: SiteQuality
SIO_000300: 1.052e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 1.44e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.09e0

DP
type: SiteQuality
SIO_000300: 3.202845e6

BaseQRankSum
type: SiteQuality
SIO_000300: 5.9e-2

MQ
type: SiteQuality
SIO_000300: 5.922e1

VQSLOD
type: SiteQuality
SIO_000300: -3.434e-1

GenotypeQuality
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bin: 1.25e1
variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

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

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

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

Latino
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allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66630
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -5.229e0

ClippingRankSum
type: SiteQuality
SIO_000300: -1.001e0

FS
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SIO_000300: 0.0e0

MQRankSum
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InbreedingCoeff
type: SiteQuality
SIO_000300: 2.1e-3

VQSLOD
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
SIO_000300: 1.01e0

QD
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.97e1

DP
type: SiteQuality
SIO_000300: 3.203075e6

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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bin: 2.25e1
variant carriers: 0

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

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.499205421126803e-5
allele num: 66702
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 5.978e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 5.8e-3

MQRankSum
type: SiteQuality
SIO_000300: 4.41e-1

QD
type: SiteQuality
SIO_000300: 8.15e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 5.649999999999999e-1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.943e0

FS
type: SiteQuality
SIO_000300: 8.89e-1

DP
type: SiteQuality
SIO_000300: 3.204299e6

ClippingRankSum
type: SiteQuality
SIO_000300: -4.98e-1

VQSLOD
type: SiteQuality
SIO_000300: 3.82e-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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bin: 8.75e1
variant carriers: 0

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

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

African
type: Population
allele count: 1
allele frequency: 9.637625289128758e-5
allele num: 10376
num of homozygotes: 0

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

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

MQRankSum
type: SiteQuality
SIO_000300: -9.86e-1

QD
type: SiteQuality
SIO_000300: 1.262e1

MQ
type: SiteQuality
SIO_000300: 5.95e1

FS
type: SiteQuality
SIO_000300: 0.0e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.8e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 7.64e-1

BaseQRankSum
type: SiteQuality
SIO_000300: 4.13e0

VQSLOD
type: SiteQuality
SIO_000300: 1.36e0

DP
type: SiteQuality
SIO_000300: 3.204237e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.3e-2

GenotypeQuality
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bin: 5.25e1
variant carriers: 0

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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bin: 9.75e1
variant carriers: 4

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

Latino
type: Population
allele count: 1
allele frequency: 8.643042350907519e-5
allele num: 11570
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: 3
allele frequency: 4.49599856128046e-5
allele num: 66726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 3.204721e6

ClippingRankSum
type: SiteQuality
SIO_000300: 8.99e-1

VQSLOD
type: SiteQuality
SIO_000300: -8.019999999999999e-2

MQRankSum
type: SiteQuality
SIO_000300: 7.93e-1

QD
type: SiteQuality
SIO_000300: 1.283e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.87e-1

MQ
type: SiteQuality
SIO_000300: 5.973e1

FS
type: SiteQuality
SIO_000300: 9.263e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.9e-3

BaseQRankSum
type: SiteQuality
SIO_000300: 6.1e-2

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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variant carriers: 0

GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
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variant carriers: 0

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

GenotypeQuality
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bin: 3.75e1
variant carriers: 0

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

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

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

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498666187093487e-5
allele num: 66726
num of homozygotes: 0

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10388
num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.914e1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.465e0

VQSLOD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: 4.4e-3

DP
type: SiteQuality
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BaseQRankSum
type: SiteQuality
SIO_000300: -6.342e0

FS
type: SiteQuality
SIO_000300: 0.0e0

ReadPosRankSum
type: SiteQuality
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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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variant carriers: 3

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

GenotypeQuality
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GenotypeQuality
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bin: 4.75e1
variant carriers: 0

European (Non-Finnish)
type: Population
allele count: 3
allele frequency: 4.496133325340207e-5
allele num: 66724
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: 8654
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
num of homozygotes: 0

South Asian
type: Population
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
allele num: 10388
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: 5.28e-1

QD
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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MQRankSum
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 1.742e0

VQSLOD
type: SiteQuality
SIO_000300: 8.5e-1

ClippingRankSum
type: SiteQuality
SIO_000300: 4.07e-1

MQ
type: SiteQuality
SIO_000300: 5.938e1

DP
type: SiteQuality
SIO_000300: 3.205076e6

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10392
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

South Asian
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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: 6614
num of homozygotes: 0

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 11570
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: 1
allele frequency: 1.155535012710885e-4
allele num: 8654
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 1.11e0

DP
type: SiteQuality
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FS
type: SiteQuality
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ReadPosRankSum
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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QD
type: SiteQuality
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BaseQRankSum
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VQSLOD
type: SiteQuality
SIO_000300: -2.157e-1

InbreedingCoeff
type: SiteQuality
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MQ
type: SiteQuality
SIO_000300: 5.902e1

GenotypeQuality
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bin: 7.5e0
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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bin: 5.25e1
variant carriers: 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
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num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

African
type: Population
allele count: 1
allele frequency: 9.622786759045419e-5
allele num: 10392
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

Latino
type: Population
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
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num of homozygotes: 0

MQ
type: SiteQuality
SIO_000300: 5.97e1

MQRankSum
type: SiteQuality
SIO_000300: 1.35e0

VQSLOD
type: SiteQuality
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BaseQRankSum
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ReadPosRankSum
type: SiteQuality
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DP
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FS
type: SiteQuality
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ClippingRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.002e1

GenotypeQuality
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bin: 2.25e1
variant carriers: 0

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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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

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

Latino
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East Asian
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South Asian
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African
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European (Non-Finnish)
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allele frequency: 2.997601918465228e-5
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Other
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QD
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DP
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VQSLOD
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ClippingRankSum
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MQ
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InbreedingCoeff
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BaseQRankSum
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MQRankSum
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FS
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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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East Asian
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Other
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num of homozygotes: 0

African
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allele frequency: 0.0e0
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Latino
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European (Non-Finnish)
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European (Finnish)
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South Asian
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MQRankSum
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MQ
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FS
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QD
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ReadPosRankSum
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ClippingRankSum
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VQSLOD
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DP
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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East Asian
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South Asian
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European (Non-Finnish)
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African
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Latino
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Other
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European (Finnish)
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ClippingRankSum
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FS
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BaseQRankSum
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MQRankSum
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InbreedingCoeff
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QD
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MQ
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VQSLOD
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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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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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allele frequency: 0.0e0
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South Asian
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Other
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Latino
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European (Non-Finnish)
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European (Finnish)
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BaseQRankSum
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MQRankSum
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ReadPosRankSum
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DP
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VQSLOD
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InbreedingCoeff
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MQ
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FS
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QD
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ClippingRankSum
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GenotypeQuality
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variant carriers: 2

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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African
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East Asian
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European (Non-Finnish)
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Latino
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European (Finnish)
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Other
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VQSLOD
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DP
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MQRankSum
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BaseQRankSum
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QD
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FS
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MQ
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ClippingRankSum
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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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African
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European (Non-Finnish)
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Other
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Latino
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South Asian
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East Asian
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European (Finnish)
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InbreedingCoeff
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FS
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ReadPosRankSum
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BaseQRankSum
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DP
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QD
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VQSLOD
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MQRankSum
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ClippingRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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South Asian
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Latino
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East Asian
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European (Non-Finnish)
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European (Finnish)
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allele num: 6614
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Other
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ClippingRankSum
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ReadPosRankSum
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QD
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FS
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InbreedingCoeff
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DP
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VQSLOD
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MQ
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MQRankSum
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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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European (Non-Finnish)
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East Asian
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African
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South Asian
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European (Finnish)
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Other
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Latino
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VQSLOD
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MQRankSum
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FS
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QD
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MQ
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BaseQRankSum
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DP
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InbreedingCoeff
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ReadPosRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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European (Finnish)
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African
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East Asian
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South Asian
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MQ
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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VQSLOD
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InbreedingCoeff
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FS
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DP
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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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European (Non-Finnish)
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African
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East Asian
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South Asian
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Latino
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InbreedingCoeff
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ReadPosRankSum
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QD
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FS
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MQ
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MQRankSum
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DP
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BaseQRankSum
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ClippingRankSum
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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European (Finnish)
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African
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European (Non-Finnish)
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South Asian
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Other
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MQ
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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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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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European (Non-Finnish)
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African
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South Asian
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East Asian
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Latino
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Other
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FS
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InbreedingCoeff
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MQ
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VQSLOD
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ReadPosRankSum
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MQRankSum
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ClippingRankSum
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QD
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BaseQRankSum
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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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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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African
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Other
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ReadPosRankSum
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InbreedingCoeff
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ClippingRankSum
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MQ
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MQRankSum
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BaseQRankSum
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FS
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DP
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QD
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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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European (Finnish)
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African
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South Asian
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European (Non-Finnish)
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East Asian
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Latino
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FS
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MQRankSum
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InbreedingCoeff
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QD
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ReadPosRankSum
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MQ
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DP
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ClippingRankSum
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VQSLOD
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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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African
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Latino
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European (Finnish)
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South Asian
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European (Non-Finnish)
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FS
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BaseQRankSum
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ClippingRankSum
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VQSLOD
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MQ
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DP
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InbreedingCoeff
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MQRankSum
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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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African
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East Asian
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European (Finnish)
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Latino
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Other
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South Asian
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MQRankSum
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QD
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ReadPosRankSum
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MQ
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FS
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ClippingRankSum
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VQSLOD
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DP
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BaseQRankSum
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InbreedingCoeff
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GenotypeQuality
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Latino
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East Asian
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African
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South Asian
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MQRankSum
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ClippingRankSum
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MQ
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InbreedingCoeff
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ReadPosRankSum
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FS
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DP
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QD
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African
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MQ
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ClippingRankSum
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VQSLOD
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DP
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FS
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MQRankSum
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BaseQRankSum
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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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Latino
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African
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European (Non-Finnish)
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allele frequency: 1.498576352465158e-5
allele num: 66730
num of homozygotes: 0

Other
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European (Finnish)
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allele frequency: 0.0e0
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East Asian
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South Asian
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VQSLOD
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InbreedingCoeff
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MQRankSum
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DP
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ClippingRankSum
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BaseQRankSum
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FS
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ReadPosRankSum
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MQ
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QD
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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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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InbreedingCoeff
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VQSLOD
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ReadPosRankSum
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BaseQRankSum
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ClippingRankSum
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MQRankSum
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MQ
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FS
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QD
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DP
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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African
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East Asian
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European (Non-Finnish)
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South Asian
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European (Finnish)
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Other
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Latino
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DP
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FS
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ReadPosRankSum
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MQ
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VQSLOD
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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QD
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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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South Asian
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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
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European (Finnish)
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African
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East Asian
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Latino
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allele frequency: 3.457216940363008e-4
allele num: 11570
num of homozygotes: 0

InbreedingCoeff
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ClippingRankSum
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MQ
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VQSLOD
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MQRankSum
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FS
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BaseQRankSum
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DP
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QD
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ReadPosRankSum
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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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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

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

Other
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num of homozygotes: 0

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

East Asian
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allele frequency: 0.0e0
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European (Finnish)
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African
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Latino
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allele frequency: 0.0e0
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European (Non-Finnish)
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allele num: 66730
num of homozygotes: 0

Other
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InbreedingCoeff
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MQRankSum
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BaseQRankSum
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MQ
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ClippingRankSum
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VQSLOD
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QD
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FS
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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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East Asian
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Latino
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European (Non-Finnish)
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allele frequency: 0.0e0
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Other
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European (Finnish)
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African
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South Asian
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InbreedingCoeff
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ClippingRankSum
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BaseQRankSum
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DP
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MQRankSum
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VQSLOD
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MQ
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Other
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European (Finnish)
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Latino
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European (Non-Finnish)
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East Asian
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African
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South Asian
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BaseQRankSum
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InbreedingCoeff
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VQSLOD
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MQ
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ClippingRankSum
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QD
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FS
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MQRankSum
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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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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Finnish)
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African
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Latino
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European (Non-Finnish)
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East Asian
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QD
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MQRankSum
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ClippingRankSum
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VQSLOD
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BaseQRankSum
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MQ
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FS
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InbreedingCoeff
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DP
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ReadPosRankSum
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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: 236

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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variant carriers: 0

GenotypeQuality
all individuals: 32
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GenotypeQuality
all individuals: 1353
bin: 7.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 4
allele frequency: 5.994844433786943e-5
allele num: 66724
num of homozygotes: 0

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

African
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allele count: 222
allele frequency: 2.134615384615384e-2
allele num: 10400
num of homozygotes: 4

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

Latino
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allele count: 11
allele frequency: 9.505703422053232e-4
allele num: 11572
num of homozygotes: 0

MQRankSum
type: SiteQuality
SIO_000300: 3.85e-1

ClippingRankSum
type: SiteQuality
SIO_000300: -1.62e-1

MQ
type: SiteQuality
SIO_000300: 5.97e1

BaseQRankSum
type: SiteQuality
SIO_000300: 1.06e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.392e1

InbreedingCoeff
type: SiteQuality
SIO_000300: 3.37e-2

DP
type: SiteQuality
SIO_000300: 3.217715e6

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.06e-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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variant carriers: 0

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

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

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

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

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

Latino
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allele count: 1
allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

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

MQ
type: SiteQuality
SIO_000300: 6.0e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.48e-1

DP
type: SiteQuality
SIO_000300: 3.216086e6

MQRankSum
type: SiteQuality
SIO_000300: 3.79e-1

VQSLOD
type: SiteQuality
SIO_000300: 7.26e-1

FS
type: SiteQuality
SIO_000300: 3.775e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 2.64e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

BaseQRankSum
type: SiteQuality
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QD
type: SiteQuality
SIO_000300: 1.235e1

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: 0

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

Other
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 906
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Latino
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allele count: 0
allele frequency: 0.0e0
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African
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allele count: 0
allele frequency: 0.0e0
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European (Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 6614
num of homozygotes: 0

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66728
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South Asian
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allele num: 16506
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.63e-1

VQSLOD
type: SiteQuality
SIO_000300: 6.879999999999999e-1

BaseQRankSum
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SIO_000300: -4.4e0

FS
type: SiteQuality
SIO_000300: 7.52e0

MQRankSum
type: SiteQuality
SIO_000300: 5.53e-1

MQ
type: SiteQuality
SIO_000300: 5.985e1

DP
type: SiteQuality
SIO_000300: 3.216232e6

QD
type: SiteQuality
SIO_000300: 1.316e1

ClippingRankSum
type: SiteQuality
SIO_000300: 1.98e-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
all individuals: 10
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variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66726
num of homozygotes: 0

African
type: Population
allele count: 3
allele frequency: 2.884615384615385e-4
allele num: 10400
num of homozygotes: 0

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

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

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

DP
type: SiteQuality
SIO_000300: 3.216449e6

BaseQRankSum
type: SiteQuality
SIO_000300: 3.91e0

MQRankSum
type: SiteQuality
SIO_000300: 8.29e-1

MQ
type: SiteQuality
SIO_000300: 5.982e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

QD
type: SiteQuality
SIO_000300: 1.33e1

FS
type: SiteQuality
SIO_000300: 5.28e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.0e0

ClippingRankSum
type: SiteQuality
SIO_000300: 4.1e-2

VQSLOD
type: SiteQuality
SIO_000300: 1.69e0

GenotypeQuality
all individuals: 30
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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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 8
allele frequency: 1.199004825994425e-4
allele num: 66722
num of homozygotes: 0

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

Latino
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allele count: 2
allele frequency: 1.728309713100588e-4
allele num: 11572
num of homozygotes: 0

African
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allele count: 3
allele frequency: 2.885725278953444e-4
allele num: 10396
num of homozygotes: 0

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

Other
type: Population
allele count: 0
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ClippingRankSum
type: SiteQuality
SIO_000300: -7.07e-1

MQRankSum
type: SiteQuality
SIO_000300: 1.99e-1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.91e-1

BaseQRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.217007e6

QD
type: SiteQuality
SIO_000300: 1.287e1

InbreedingCoeff
type: SiteQuality
SIO_000300: -3.0e-4

VQSLOD
type: SiteQuality
SIO_000300: 3.55e0

FS
type: SiteQuality
SIO_000300: 5.34e-1

MQ
type: SiteQuality
SIO_000300: 5.971e1

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

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

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

Latino
type: Population
allele count: 0
allele frequency: 0.0e0
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Other
type: Population
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allele frequency: 0.0e0
allele num: 906
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African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

DP
type: SiteQuality
SIO_000300: 3.216797e6

VQSLOD
type: SiteQuality
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BaseQRankSum
type: SiteQuality
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InbreedingCoeff
type: SiteQuality
SIO_000300: -2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 3.91e-1

FS
type: SiteQuality
SIO_000300: 7.226e0

MQRankSum
type: SiteQuality
SIO_000300: 4.82e-1

MQ
type: SiteQuality
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QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: 9.07e-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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variant carriers: 0

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

Other
type: Population
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allele num: 906
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East Asian
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allele frequency: 0.0e0
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South Asian
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allele frequency: 0.0e0
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Latino
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African
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allele frequency: 9.617234083477592e-5
allele num: 10398
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European (Finnish)
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allele count: 0
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VQSLOD
type: SiteQuality
SIO_000300: 8.37e-1

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

MQRankSum
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DP
type: SiteQuality
SIO_000300: 3.216829e6

GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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South Asian
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European (Non-Finnish)
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allele count: 2
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allele num: 66718
num of homozygotes: 0

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

European (Finnish)
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allele frequency: 0.0e0
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African
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Other
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VQSLOD
type: SiteQuality
SIO_000300: 6.08e-1

FS
type: SiteQuality
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ReadPosRankSum
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MQRankSum
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MQ
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DP
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InbreedingCoeff
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ClippingRankSum
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QD
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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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Latino
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num of homozygotes: 0

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

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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South Asian
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allele frequency: 7.875923906458257e-4
allele num: 16506
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MQ
type: SiteQuality
SIO_000300: 5.972e1

InbreedingCoeff
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BaseQRankSum
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ReadPosRankSum
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DP
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SIO_000300: 3.216841e6

ClippingRankSum
type: SiteQuality
SIO_000300: -5.16e-1

FS
type: SiteQuality
SIO_000300: 1.77e0

VQSLOD
type: SiteQuality
SIO_000300: -6.356000000000001e-1

MQRankSum
type: SiteQuality
SIO_000300: -6.46e-1

QD
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GenotypeQuality
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bin: 2.5e0
variant carriers: 0

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

GenotypeQuality
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bin: 7.25e1
variant carriers: 0

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

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

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

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

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498711108446736e-5
allele num: 66724
num of homozygotes: 0

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

BaseQRankSum
type: SiteQuality
SIO_000300: -3.089e0

ClippingRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQRankSum
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SIO_000300: -1.187e0

MQ
type: SiteQuality
SIO_000300: 5.985e1

ReadPosRankSum
type: SiteQuality
SIO_000300: 7.11e-1

VQSLOD
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InbreedingCoeff
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SIO_000300: 0.0e0

FS
type: SiteQuality
SIO_000300: 1.1076e1

DP
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

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

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

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

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

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

European (Non-Finnish)
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allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

DP
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SIO_000300: 3.216828e6

ClippingRankSum
type: SiteQuality
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FS
type: SiteQuality
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MQ
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BaseQRankSum
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InbreedingCoeff
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SIO_000300: 1.0e-4

MQRankSum
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SIO_000300: 1.29e0

ReadPosRankSum
type: SiteQuality
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VQSLOD
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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

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

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

Latino
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allele frequency: 8.641548565502938e-5
allele num: 11572
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66718
num of homozygotes: 0

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

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

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

MQ
type: SiteQuality
SIO_000300: 5.959e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.186e0

MQRankSum
type: SiteQuality
SIO_000300: 1.29e0

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: 6.3e-1

QD
type: SiteQuality
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ClippingRankSum
type: SiteQuality
SIO_000300: -4.1e-1

FS
type: SiteQuality
SIO_000300: 2.031e0

VQSLOD
type: SiteQuality
SIO_000300: 5.04e-1

DP
type: SiteQuality
SIO_000300: 3.216828e6

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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bin: 3.25e1
variant carriers: 0

African
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allele count: 1
allele frequency: 9.617234083477592e-5
allele num: 10398
num of homozygotes: 0

European (Non-Finnish)
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 66722
num of homozygotes: 0

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

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

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

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

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

BaseQRankSum
type: SiteQuality
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QD
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MQ
type: SiteQuality
SIO_000300: 5.984e1

VQSLOD
type: SiteQuality
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FS
type: SiteQuality
SIO_000300: 5.971e0

ClippingRankSum
type: SiteQuality
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DP
type: SiteQuality
SIO_000300: 3.217041e6

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.0e-4

ReadPosRankSum
type: SiteQuality
SIO_000300: -9.1e-2

MQRankSum
type: SiteQuality
SIO_000300: 5.19e-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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variant carriers: 0

GenotypeQuality
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variant carriers: 0

European (Non-Finnish)
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allele count: 1
allele frequency: 1.498756032493031e-5
allele num: 66722
num of homozygotes: 0

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

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

African
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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

South Asian
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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: 0.0e0
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num of homozygotes: 0

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

European (Non-Finnish)
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allele count: 2
allele frequency: 2.997512064986062e-5
allele num: 66722
num of homozygotes: 0

African
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allele count: 0
allele frequency: 0.0e0
allele num: 10398
num of homozygotes: 0

Latino
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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
allele num: 16500
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European (Finnish)
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allele frequency: 1.511944360447536e-4
allele num: 6614
num of homozygotes: 0

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

Other
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allele frequency: 0.0e0
allele num: 906
num of homozygotes: 0

InbreedingCoeff
type: SiteQuality
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DP
type: SiteQuality
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BaseQRankSum
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FS
type: SiteQuality
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ClippingRankSum
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MQRankSum
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QD
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VQSLOD
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ReadPosRankSum
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MQ
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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GenotypeQuality
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Latino
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allele count: 0
allele frequency: 0.0e0
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num of homozygotes: 0

Other
type: Population
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allele frequency: 0.0e0
allele num: 906
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European (Non-Finnish)
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allele count: 2
allele frequency: 2.997601918465228e-5
allele num: 66720
num of homozygotes: 0

African
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East Asian
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allele num: 8654
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South Asian
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European (Finnish)
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allele count: 1
allele frequency: 1.512401693889897e-4
allele num: 6612
num of homozygotes: 0

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

South Asian
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African
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Latino
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East Asian
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European (Finnish)
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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
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num of homozygotes: 0

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

European (Finnish)
type: Population
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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South Asian
type: Population
allele count: 0
allele frequency: 0.0e0
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European (Non-Finnish)
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allele count: 1
allele frequency: 1.498800959232614e-5
allele num: 66720
num of homozygotes: 0

East Asian
type: Population
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Other
type: Population
allele count: 0
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num of homozygotes: 0

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

ReadPosRankSum
type: SiteQuality
SIO_000300: 1.79e0

BaseQRankSum
type: SiteQuality
SIO_000300: -3.854e0

FS
type: SiteQuality
SIO_000300: 5.236e0

DP
type: SiteQuality
SIO_000300: 3.217065e6

VQSLOD
type: SiteQuality
SIO_000300: -4.666e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: -1.0e-4

MQRankSum
type: SiteQuality
SIO_000300: -2.71e-1

MQ
type: SiteQuality
SIO_000300: 5.905e1

QD
type: SiteQuality
SIO_000300: 1.479e1

ClippingRankSum
type: SiteQuality
SIO_000300: -2.182e0

GenotypeQuality
all individuals: 1645
bin: 7.75e1
variant carriers: 0

GenotypeQuality
all individuals: 39
bin: 3.25e1
variant carriers: 0

GenotypeQuality
all individuals: 2034
bin: 6.75e1
variant carriers: 0

GenotypeQuality
all individuals: 43282
bin: 9.75e1
variant carriers: 1

GenotypeQuality
all individuals: 2170
bin: 9.25e1
variant carriers: 0

GenotypeQuality
all individuals: 20
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 69
bin: 2.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 25
bin: 5.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 45
bin: 3.75e1
variant carriers: 0

GenotypeQuality
all individuals: 6455
bin: 6.25e1
variant carriers: 0

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

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

European (Non-Finnish)
type: Population
allele count: 1
allele frequency: 1.498845888665727e-5
allele num: 66718
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: 11574
num of homozygotes: 0

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

African
type: Population
allele count: 0
allele frequency: 0.0e0
allele num: 10394
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: -1.022e0

QD
type: SiteQuality
SIO_000300: 1.222e1

BaseQRankSum
type: SiteQuality
SIO_000300: -3.958e0

MQ
type: SiteQuality
SIO_000300: 5.963e1

VQSLOD
type: SiteQuality
SIO_000300: 4.68e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 1.6e-3

DP
type: SiteQuality
SIO_000300: 3.217335e6

FS
type: SiteQuality
SIO_000300: 5.937e0

ClippingRankSum
type: SiteQuality
SIO_000300: 2.14e0

ReadPosRankSum
type: SiteQuality
SIO_000300: -1.352e0

GenotypeQuality
all individuals: 3
bin: 1.75e1
variant carriers: 0

GenotypeQuality
all individuals: 1356
bin: 7.25e1
variant carriers: 0

GenotypeQuality
all individuals: 32
bin: 4.25e1
variant carriers: 0

GenotypeQuality
all individuals: 43282
bin: 9.75e1
variant carriers: 2

GenotypeQuality
all individuals: 2169
bin: 9.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 6463
bin: 6.25e1
variant carriers: 0

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

GenotypeQuality
all individuals: 24
bin: 5.75e1
variant carriers: 0

GenotypeQuality
all individuals: 28
bin: 5.25e1
variant carriers: 0

GenotypeQuality
all individuals: 36
bin: 4.75e1
variant carriers: 0

GenotypeQuality
all individuals: 40
bin: 3.75e1
variant carriers: 0

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

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

South Asian
type: Population
allele count: 1
allele frequency: 6.05913717886573e-5
allele num: 16504
num of homozygotes: 0

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

Other
type: Population
allele count: 0
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: 66718
num of homozygotes: 0

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

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

DP
type: SiteQuality
SIO_000300: 3.217327e6

MQRankSum
type: SiteQuality
SIO_000300: 1.46e-1

InbreedingCoeff
type: SiteQuality
SIO_000300: 2.2e-3

ClippingRankSum
type: SiteQuality
SIO_000300: 1.79e0

QD
type: SiteQuality
SIO_000300: 1.503e1

MQ
type: SiteQuality
SIO_000300: 6.0e1

BaseQRankSum
type: SiteQuality
SIO_000300: -1.29e0

ReadPosRankSum
type: SiteQuality
SIO_000300: 4.28e-1

FS
type: SiteQuality
SIO_000300: 0.0e0

VQSLOD
type: SiteQuality
SIO_000300: 5.28e0